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rs121908321

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908321(C;T)
Make rs121908321(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position9890687
GeneSLC2A9
is asnp
is mentioned by
dbSNPrs121908321
ebirs121908321
HLIrs121908321
Exacrs121908321
Varsomers121908321
Maprs121908321
PheGenIrs121908321
hapmaprs121908321
1000 genomesrs121908321
hgdprs121908321
ensemblrs121908321
gopubmedrs121908321
geneviewrs121908321
scholarrs121908321
googlers121908321
pharmgkbrs121908321
gwascentralrs121908321
openSNPrs121908321
23andMers121908321
23andMe allrs121908321
SNP Nexus

SNPshotrs121908321
SNPdbers121908321
MSV3drs121908321
GWAS Ctlgrs121908321
Max Magnitude0
OMIM606142
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121908321(A,T;A,T)
Alt rs121908321(A,T;A,T)
Reference rs121908321(C;C)
Significance Pathogenic
Disease Renal hypouricemia 2
Variation info
Gene SLC2A9
CLNDBN Renal hypouricemia 2
Reversed 1
HGVS NC_000004.11:g.9892311G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000004859.2,