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rs776127501

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs776127501(A;A)
Make rs776127501(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position9985693
GeneSLC2A9
is asnp
is mentioned by
dbSNPrs776127501
ebirs776127501
HLIrs776127501
Exacrs776127501
Varsomers776127501
Maprs776127501
PheGenIrs776127501
hapmaprs776127501
1000 genomesrs776127501
hgdprs776127501
ensemblrs776127501
gopubmedrs776127501
geneviewrs776127501
scholarrs776127501
googlers776127501
pharmgkbrs776127501
gwascentralrs776127501
openSNPrs776127501
23andMers776127501
23andMe allrs776127501
SNP Nexus

SNPshotrs776127501
SNPdbers776127501
MSV3drs776127501
GWAS Ctlgrs776127501
Max Magnitude0
ClinVar
Risk rs776127501(A;A)
Alt rs776127501(A;A)
Reference rs776127501(G;G)
Significance Pathogenic
Disease Renal hypouricemia 2
Variation info
Gene SLC2A9
CLNDBN Renal hypouricemia 2
Reversed 0
HGVS NC_000004.11:g.9987317G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000201281.1,