Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: ESR1 (Hsa)
(GRCh38)6:151808634C>G
(Homo sapiens)Allele/Variant
Source: rs73780865
Genes: ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:151808634C>G
(GRCh38)6:151842613C>T
(Homo sapiens)Allele/Variant
Source: rs104893956
Genes: ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, stop_gained, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:151842613C>T
(GRCh38)6:151880329T>C
(Homo sapiens)Allele/Variant
Source: rs6557169
Genes: ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:151880329T>C
(GRCh38)6:151944217C>T
(Homo sapiens)Allele/Variant
Source: rs142712646
Genes: ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:151944217C>T
(GRCh38)6:152122250C>T
(Homo sapiens)Allele/Variant
Source: rs766338162
Genes: SYNE1 (Hsa), ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152122250C>T
(GRCh38)6:152122439G>A
(Homo sapiens)Allele/Variant
Source: rs201891399
Genes: SYNE1 (Hsa), ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152122439G>A
(GRCh38)6:152122692A>T
(Homo sapiens)Allele/Variant
Source: rs1211583568
Genes: SYNE1 (Hsa), ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152122692A>T
(GRCh38)6:152122500G>C
(Homo sapiens)Allele/Variant
Source: rs377446250
Genes: SYNE1 (Hsa), ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152122500G>C
(GRCh38)6:152094402T>C
(Homo sapiens)Allele/Variant
Source: rs1057519714
Genes: ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152094402T>C
(GRCh38)6:152122618G>A
(Homo sapiens)Allele/Variant
Source: rs144206837
Genes: SYNE1 (Hsa), ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152122618G>A
(GRCh38)6:152017301G>A
(Homo sapiens)Allele/Variant
Source: rs207467519
Genes: ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152017301G>A
(GRCh38)6:151880856G>A
(Homo sapiens)Allele/Variant
Source: rs9340846
Genes: ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:151880856G>A
(GRCh38)6:152121987A>T
(Homo sapiens)Allele/Variant
Source: rs886061188
Genes: SYNE1 (Hsa), ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152121987A>T
(GRCh38)6:152122003T>C
(Homo sapiens)Allele/Variant
Source: rs886061189
Genes: SYNE1 (Hsa), ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152122003T>C
(GRCh38)6:152122635C>T
(Homo sapiens)Allele/Variant
Source: rs1554349162
Genes: SYNE1 (Hsa), ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152122635C>T
(GRCh38)6:151944524G>A
(Homo sapiens)Allele/Variant
Source: rs9397459
Genes: ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:151944524G>A
(GRCh38)6:152122657C>T
(Homo sapiens)Allele/Variant
Source: rs767663894
Genes: SYNE1 (Hsa), ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152122657C>T
(GRCh38)6:152122485C>T
(Homo sapiens)Allele/Variant
Source: rs550697327
Genes: SYNE1 (Hsa), ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152122485C>T
(GRCh38)6:152122553G>A
(Homo sapiens)Allele/Variant
Source: rs200240881
Genes: SYNE1 (Hsa), ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152122553G>A
(GRCh38)6:152122558G>C
(Homo sapiens)Allele/Variant
Source: rs139740651
Genes: SYNE1 (Hsa), ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152122558G>C
(GRCh38)6:152099262A>G
(Homo sapiens)Allele/Variant
Source: rs35151682
Genes: ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152099262A>G
(GRCh38)6:151807942T>C
(Homo sapiens)Allele/Variant
Source: rs2077647
Genes: ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)6:151807942T>C
(GRCh38)6:151944503T>A
(Homo sapiens)Allele/Variant
Source: rs121913044
Genes: ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:151944503T>A
(GRCh38)6:152011561A>G
(Homo sapiens)Allele/Variant
Source: rs9340973
Genes: ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152011561A>G
(GRCh38)6:152121987A>G
(Homo sapiens)Allele/Variant
Source: rs886061188
Genes: SYNE1 (Hsa), ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152121987A>G
(GRCh38)6:152122686G>T
(Homo sapiens)Allele/Variant
Source: rs749838365
Genes: SYNE1 (Hsa), ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152122686G>T
(GRCh38)6:152122542C>T
(Homo sapiens)Allele/Variant
Source: rs759447071
Genes: SYNE1 (Hsa), ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152122542C>T
(GRCh38)6:152122551C>T
(Homo sapiens)Allele/Variant
Source: rs747635401
Genes: SYNE1 (Hsa), ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152122551C>T
(GRCh38)6:151808208C>T
(Homo sapiens)Allele/Variant
Source: NC_000006.12:g.151808208C>T
Genes: ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:151808208C>T
(GRCh38)6:151808227G>A
(Homo sapiens)Allele/Variant
Source: rs181468071
Genes: ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)6:151808227G>A
(GRCh38)6:152060863T>C
(Homo sapiens)Allele/Variant
Source: rs9341016
Genes: ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152060863T>C
(GRCh38)6:152122658G>A
(Homo sapiens)Allele/Variant
Source: rs551962186
Genes: SYNE1 (Hsa), ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, stop_gained, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152122658G>A
(GRCh38)6:152122685A>G
(Homo sapiens)Allele/Variant
Source: rs922921602
Genes: SYNE1 (Hsa), ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152122685A>G
(GRCh38)6:152122505G>C
(Homo sapiens)Allele/Variant
Source: rs1198815454
Genes: SYNE1 (Hsa), ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152122505G>C
(GRCh38)6:152121686C>A
(Homo sapiens)Allele/Variant
Source: rs2813558
Genes: SYNE1 (Hsa), ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152121686C>A
(GRCh38)6:151808188C>T
(Homo sapiens)Allele/Variant
Source: rs1427814349
Genes: ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)6:151808188C>T
(GRCh38)6:152011690C>T
(Homo sapiens)Allele/Variant
Source: rs61760169
Genes: ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152011690C>T
(GRCh38)6:151842600A>G
(Homo sapiens)Allele/Variant
Source: rs758203894
Genes: ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:151842600A>G
(GRCh38)6:152122594G>A
(Homo sapiens)Allele/Variant
Source: rs746177326
Genes: SYNE1 (Hsa), ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152122594G>A
(GRCh38)6:151944444C>T
(Homo sapiens)Allele/Variant
Source: rs144223995
Genes: ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:151944444C>T
(GRCh38)6:152098960G>A
(Homo sapiens)Allele/Variant
Source: rs2228480
Genes: ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152098960G>A
(GRCh38)6:152122068A>G
(Homo sapiens)Allele/Variant
Source: rs927168592
Genes: SYNE1 (Hsa), ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152122068A>G
(GRCh38)6:152122650G>A
(Homo sapiens)Allele/Variant
Source: rs1585315718
Genes: SYNE1 (Hsa), ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152122650G>A
(GRCh38)6:152122672T>A
(Homo sapiens)Allele/Variant
Source: rs780263411
Genes: SYNE1 (Hsa), ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152122672T>A
(GRCh38)6:152122460G>T
(Homo sapiens)Allele/Variant
Source: rs777985131
Genes: SYNE1 (Hsa), ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152122460G>T
(GRCh38)6:152011969G>A
(Homo sapiens)Allele/Variant
Source: rs13203975
Genes: ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152011969G>A
(GRCh38)6:151808453C>T
(Homo sapiens)Allele/Variant
Source: rs6914438
Genes: ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:151808453C>T
(GRCh38)6:151808208C>A
(Homo sapiens)Allele/Variant
Source: rs773500294
Genes: ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:151808208C>A
(GRCh38)6:151808318C>T
(Homo sapiens)Allele/Variant
Source: rs201145204
Genes: ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:151808318C>T
(GRCh38)6:152098933G>A
(Homo sapiens)Allele/Variant
Source: rs150547091
Genes: ESR1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:152098933G>A