rs1799989

plus

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

Make rs1799989(A;A)

Reference

GRCh38 38.1/141

Chromosome

11

Position

89177755

Gene	LOC107984363, TYR

is a	snp
is	mentioned by
dbSNP	rs1799989
dbSNP (classic)	rs1799989
ClinGen	rs1799989
ebi	rs1799989
HLI	rs1799989
Exac	rs1799989
Gnomad	rs1799989
Varsome	rs1799989
LitVar	rs1799989
Map	rs1799989
PheGenI	rs1799989
Biobank	rs1799989
1000 genomes	rs1799989
hgdp	rs1799989
ensembl	rs1799989
geneview	rs1799989
scholar	rs1799989
google	rs1799989
pharmgkb	rs1799989
gwascentral	rs1799989
openSNP	rs1799989
23andMe	rs1799989
SNPshot	rs1799989
SNPdbe	rs1799989
MSV3d	rs1799989
GWAS Ctlg	rs1799989

GMAF

0.1694

Max Magnitude

0.5

?

(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 17999355 ] A genomewide association study of skin pigmentation in a South Asian population.