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rs121908323

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908323(C;G)
Make rs121908323(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position9887623
GeneSLC2A9
is asnp
is mentioned by
dbSNPrs121908323
ebirs121908323
HLIrs121908323
Exacrs121908323
Varsomers121908323
Maprs121908323
PheGenIrs121908323
hapmaprs121908323
1000 genomesrs121908323
hgdprs121908323
ensemblrs121908323
gopubmedrs121908323
geneviewrs121908323
scholarrs121908323
googlers121908323
pharmgkbrs121908323
gwascentralrs121908323
openSNPrs121908323
23andMers121908323
23andMe allrs121908323
SNP Nexus

SNPshotrs121908323
SNPdbers121908323
MSV3drs121908323
GWAS Ctlgrs121908323
Max Magnitude0
OMIM606142
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121908323(G;G)
Alt rs121908323(G;G)
Reference rs121908323(C;C)
Significance Pathogenic
Disease Renal hypouricemia 2
Variation info
Gene SLC2A9
CLNDBN Renal hypouricemia 2
Reversed 1
HGVS NC_000004.11:g.9889247G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000004861.2,