Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: DRD2 (Hsa)
(GRCh38)11:113424254T>C
(Homo sapiens)Allele/Variant
Source: rs11608185
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113424254T>C
(GRCh38)11:113415194C>T
(Homo sapiens)Allele/Variant
Source: rs12363125
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113415194C>T
(GRCh38)11:113410754C>T
(Homo sapiens)Allele/Variant
Source: rs77930100
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113410754C>T
(GRCh38)11:113412715T>C
(Homo sapiens)Allele/Variant
Source: rs71653614
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113412715T>C
(GRCh38)11:113412766G>A
(Homo sapiens)Allele/Variant
Source: rs1800496
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113412766G>A
(GRCh38)11:113410767A>G
(Homo sapiens)Allele/Variant
Source: rs376186482
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113410767A>G
(GRCh38)11:113410799G>A
(Homo sapiens)Allele/Variant
Source: rs200440686
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113410799G>A
(GRCh38)11:113424592C>T
(Homo sapiens)Allele/Variant
Source: rs4986923
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113424592C>T
(GRCh38)11:113412573A>C
(Homo sapiens)Allele/Variant
Source: rs2138156316
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113412573A>C
(GRCh38)11:113412762G>C
(Homo sapiens)Allele/Variant
Source: rs1801028
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113412762G>C
(GRCh38)11:113411128C>T
(Homo sapiens)Allele/Variant
Source: rs77142532
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113411128C>T
(GRCh38)11:113418460T>C
(Homo sapiens)Allele/Variant
Source: rs1079727
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113418460T>C
(GRCh38)11:113424360C>T
(Homo sapiens)Allele/Variant
Source: rs76985854
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113424360C>T
(GRCh38)11:113412654G>A
(Homo sapiens)Allele/Variant
Source: rs144999500
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113412654G>A
(GRCh38)11:113412755A>G
(Homo sapiens)Allele/Variant
Source: rs6275
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113412755A>G
(GRCh38)11:113414404C>T
(Homo sapiens)Allele/Variant
Source: rs1415830775
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113414404C>T
(GRCh38)11:113414444G>T
(Homo sapiens)Allele/Variant
Source: NC_000011.10:g.113414444G>T
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113414444G>T
(GRCh38)11:113416935C>T
(Homo sapiens)Allele/Variant
Source: rs104894220
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113416935C>T
(GRCh38)11:113418032G>A
(Homo sapiens)Allele/Variant
Source: rs750801533
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113418032G>A
(GRCh38)11:113415615G>A
(Homo sapiens)Allele/Variant
Source: rs202133725
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113415615G>A
(GRCh38)11:113412491A>C
(Homo sapiens)Allele/Variant
Source: rs57666437
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113412491A>C
(GRCh38)11:113412958T>C
(Homo sapiens)Allele/Variant
Source: rs1076561
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113412958T>C
(GRCh38)11:113410711C>T
(Homo sapiens)Allele/Variant
Source: rs199523375
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113410711C>T
(GRCh38)11:113412824G>C
(Homo sapiens)Allele/Variant
Source: rs74548208
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113412824G>C
(GRCh38)11:113424421T>C
(Homo sapiens)Allele/Variant
Source: rs202172997
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113424421T>C
(GRCh38)11:113412671A>G
(Homo sapiens)Allele/Variant
Source: rs1054271642
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113412671A>G
(GRCh38)11:113412728G>A
(Homo sapiens)Allele/Variant
Source: rs143935143
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113412728G>A
(GRCh38)11:113416972C>T
(Homo sapiens)Allele/Variant
Source: rs1800499
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113416972C>T
(GRCh38)11:113417007G>T
(Homo sapiens)Allele/Variant
Source: rs1359352412
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113417007G>T
(GRCh38)11:113418092G>A
(Homo sapiens)Allele/Variant
Source: rs201130366
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113418092G>A
(GRCh38)11:113412966C>A
(Homo sapiens)Allele/Variant
Source: rs1076560
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113412966C>A
(GRCh38)11:113424977G>A
(Homo sapiens)Allele/Variant
Source: rs79723153
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113424977G>A
(GRCh38)11:113412651T>C
(Homo sapiens)Allele/Variant
Source: rs143779712
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113412651T>C
(GRCh38)11:113417010G>A
(Homo sapiens)Allele/Variant
Source: rs537699837
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113417010G>A
(GRCh38)11:113418062C>G
(Homo sapiens)Allele/Variant
Source: rs199754592
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113418062C>G
(GRCh38)11:113412814G>A
(Homo sapiens)Allele/Variant
Source: rs758884516
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113412814G>A
(GRCh38)11:113412836G>A
(Homo sapiens)Allele/Variant
Source: rs772030347
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113412836G>A
(GRCh38)11:113412873C>T
(Homo sapiens)Allele/Variant
Source: rs200184730
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113412873C>T
(GRCh38)11:113424501C>T
(Homo sapiens)Allele/Variant
Source: rs1950919208
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113424501C>T
(GRCh38)11:113412752A>G
(Homo sapiens)Allele/Variant
Source: rs909622147
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113412752A>G
(GRCh38)11:113418133C>T
(Homo sapiens)Allele/Variant
Source: NC_000011.10:g.113418133C>T
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113418133C>T
(GRCh38)11:113416156T>C
(Homo sapiens)Allele/Variant
Source: rs2440390
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113416156T>C
(GRCh38)11:113412764C>T
(Homo sapiens)Allele/Variant
Source: rs201422791
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113412764C>T
(GRCh38)11:113416789G>T
(Homo sapiens)Allele/Variant
Source: rs35352421
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113416789G>T
(GRCh38)11:113424539G>A
(Homo sapiens)Allele/Variant
Source: rs767413934
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113424539G>A
(GRCh38)11:113414444G>C
(Homo sapiens)Allele/Variant
Source: rs80350280
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113414444G>C
(GRCh38)11:113424520G>A
(Homo sapiens)Allele/Variant
Source: rs4986918
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113424520G>A
(GRCh38)11:113414814C>A
(Homo sapiens)Allele/Variant
Source: rs2283265
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113414814C>A
(GRCh38)11:113411054A>C
(Homo sapiens)Allele/Variant
Source: rs2734841
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113411054A>C
(GRCh38)11:113415464C>T
(Homo sapiens)Allele/Variant
Source: rs371023969
Genes: DRD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:113415464C>T