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rs589691

From SNPedia

Orientationplus
Stabilizedplus
Make rs589691(C;C)
Make rs589691(C;T)
Make rs589691(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position64757744
GenePYGM, RASGRP2
is asnp
is mentioned by
dbSNPrs589691
ebirs589691
HLIrs589691
Exacrs589691
Varsomers589691
Maprs589691
PheGenIrs589691
hapmaprs589691
1000 genomesrs589691
hgdprs589691
ensemblrs589691
gopubmedrs589691
geneviewrs589691
scholarrs589691
googlers589691
pharmgkbrs589691
gwascentralrs589691
openSNPrs589691
23andMers589691
23andMe allrs589691
SNP Nexus

SNPshotrs589691
SNPdbers589691
MSV3drs589691
GWAS Ctlgrs589691
GMAF0.3563
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21768215OA-icon.png]
Trait
Title Genome-wide association study for serum urate concentrations and gout among African Americans identifies genomic risk loci and a novel URAT1 loss-of-function allele.
Risk Allele T
P-val 9E-8
Odds Ratio 0.1500 [NR] mg/dl decrease


ClinVar
Risk rs589691(T;T)
Alt rs589691(T;T)
Reference rs589691(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene PYGM
CLNDBN not specified
Reversed 0
HGVS NC_000011.9:g.64525216C>T
CLNSRC
CLNACC RCV000252745.1,