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rs1799989

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;C) 0.5 benign most likely
(C;C) 0 common in clinvar


Make rs1799989(A;A)
ReferenceGRCh38 38.1/141
Chromosome11
Position89177755
GeneTYR
is asnp
is mentioned by
dbSNPrs1799989
ebirs1799989
HLIrs1799989
Exacrs1799989
Varsomers1799989
Maprs1799989
PheGenIrs1799989
hapmaprs1799989
1000 genomesrs1799989
hgdprs1799989
ensemblrs1799989
gopubmedrs1799989
geneviewrs1799989
scholarrs1799989
googlers1799989
pharmgkbrs1799989
gwascentralrs1799989
openSNPrs1799989
23andMers1799989
23andMe allrs1799989
SNP Nexus

SNPshotrs1799989
SNPdbers1799989
MSV3drs1799989
GWAS Ctlgrs1799989
GMAF0.1694
Max Magnitude0.5
? (A;A) (A;C) (C;C) 28
[PMID 18855532] among 120 (likely Japanese) first-episode neuroleptic-naive schizophrenics treated with risperidone genotyped for 30 variants in misc. dopamine and serotonin (receptors and otherwise) two SNPs in DRD2 (rs1799989 and rs1800497) and two SNPs in AKT1 (rs3803300 and rs2494732) were significant predictors of treatment response to risperidone


ClinVar
Risk rs1799989(A;A)
Alt rs1799989(A;A)
Reference Rs1799989(C;C)
Significance Non-pathogenic
Disease Tyrosinase-negative oculocutaneous albinism not provided
Variation info
Gene TYR
CLNDBN Tyrosinase-negative oculocutaneous albinism not provided
Reversed 0
HGVS NC_000011.9:g.88910923C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003986.4, RCV000085882.1,



[PMID 17999355OA-icon.png] A genomewide association study of skin pigmentation in a South Asian population.