Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: SNCA (Hsa) Molecular Consequence: non coding transcript exon variant
(GRCh38)4:89822180C>T
(Homo sapiens)Allele/Variant
Source: rs10005233
Genes: SNCA (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)4:89822180C>T
(GRCh38)4:89835536G>A
(Homo sapiens)Allele/Variant
Source: rs35135226
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835536G>A
(GRCh38)4:89726714T>C
(Homo sapiens)Allele/Variant
Source: rs6842093
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89726714T>C
(GRCh38)4:89746090C>G
(Homo sapiens)Allele/Variant
Source: rs207464865
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89746090C>G
(GRCh38)4:89729187C>G
(Homo sapiens)Allele/Variant
Source: rs370797923
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89729187C>G
(GRCh38)4:89822239G>A
(Homo sapiens)Allele/Variant
Source: rs2110460139
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822239G>A
(GRCh38)4:89822704C>G
(Homo sapiens)Allele/Variant
Source: rs7356228
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822704C>G
(GRCh38)4:89828284T>G
(Homo sapiens)Allele/Variant
Source: rs34183114
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89828284T>G
(GRCh38)4:89835475C>T
(Homo sapiens)Allele/Variant
Source: rs35009676
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835475C>T
(GRCh38)4:89729158A>G
(Homo sapiens)Allele/Variant
Source: rs144274752
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89729158A>G
(GRCh38)4:89836947G>A
(Homo sapiens)Allele/Variant
Source: rs545809130
Genes: SNCA-AS1 (Hsa), SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89836947G>A
(GRCh38)4:89837155C>G
(Homo sapiens)Allele/Variant
Source: rs757451373
Genes: SNCA-AS1 (Hsa), SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89837155C>G
(GRCh38)4:89837187T>G
(Homo sapiens)Allele/Variant
Source: rs767878442
Genes: SNCA-AS1 (Hsa), SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89837187T>G
(GRCh38)4:89828186T>G
(Homo sapiens)Allele/Variant
Source: rs2110488615
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_acceptor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89828186T>G
(GRCh38)4:89828320T>A
(Homo sapiens)Allele/Variant
Source: rs554831708
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89828320T>A
(GRCh38)4:89836976C>T
(Homo sapiens)Allele/Variant
Source: rs886059729
Genes: SNCA-AS1 (Hsa), SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89836976C>T
(GRCh38)4:89827981A>G
(Homo sapiens)Allele/Variant
Source: rs1442149
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89827981A>G
(GRCh38)4:89828136A>C
(Homo sapiens)Allele/Variant
Source: rs1578405610
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89828136A>C
(GRCh38)4:89828137G>T
(Homo sapiens)Allele/Variant
Source: rs2110488377
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89828137G>T
(GRCh38)4:89822496A>T
(Homo sapiens)Allele/Variant
Source: rs11944927
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822496A>T
(GRCh38)4:89835270G>C
(Homo sapiens)Allele/Variant
Source: rs2028535
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835270G>C
(GRCh38)4:89836955C>T
(Homo sapiens)Allele/Variant
Source: rs548276692
Genes: SNCA-AS1 (Hsa), SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89836955C>T
(GRCh38)4:89729290G>A
(Homo sapiens)Allele/Variant
Source: rs763527339
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89729290G>A
(GRCh38)4:89729183T>G
(Homo sapiens)Allele/Variant
Source: rs546366532
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89729183T>G
(GRCh38)4:89822226C>T
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.89822226C>T
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822226C>T
(GRCh38)4:89822404A>T
(Homo sapiens)Allele/Variant
Source: rs762146888
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822404A>T
(GRCh38)4:89836961C>T
(Homo sapiens)Allele/Variant
Source: rs1560562993
Genes: SNCA-AS1 (Hsa), SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, splice_donor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89836961C>T
(GRCh38)4:89726676T>C
(Homo sapiens)Allele/Variant
Source: rs371014092
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89726676T>C
(GRCh38)4:89822238A>G
(Homo sapiens)Allele/Variant
Source: rs758513669
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822238A>G
(GRCh38)4:89827937T>C
(Homo sapiens)Allele/Variant
Source: rs36014224
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89827937T>C
(GRCh38)4:89835382C>T
(Homo sapiens)Allele/Variant
Source: rs141771108
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835382C>T
(GRCh38)4:89835399C>G
(Homo sapiens)Allele/Variant
Source: rs7681440
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835399C>G
(GRCh38)4:89835534G>A
(Homo sapiens)Allele/Variant
Source: rs763539470
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835534G>A
(GRCh38)4:89837051G>C
(Homo sapiens)Allele/Variant
Source: rs926228768
Genes: SNCA-AS1 (Hsa), SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89837051G>C
(GRCh38)4:89837063G>A
(Homo sapiens)Allele/Variant
Source: rs764272411
Genes: SNCA-AS1 (Hsa), SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89837063G>A
(GRCh38)4:89726674A>G
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.89726674A>G
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89726674A>G
(GRCh38)4:89835538T>G
(Homo sapiens)Allele/Variant
Source: rs374658468
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835538T>G
(GRCh38)4:89837065C>T
(Homo sapiens)Allele/Variant
Source: rs367902113
Genes: SNCA-AS1 (Hsa), SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89837065C>T
(GRCh38)4:89836978A>G
(Homo sapiens)Allele/Variant
Source: rs886059730
Genes: SNCA-AS1 (Hsa), SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89836978A>G
(GRCh38)4:89837210C>T
(Homo sapiens)Allele/Variant
Source: rs372025454
Genes: SNCA-AS1 (Hsa), SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89837210C>T
(GRCh38)4:89726667T>C
(Homo sapiens)Allele/Variant
Source: rs2110065158
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89726667T>C