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rs121917743

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121917743(G;G)
Make rs121917743(G;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position204166247
GeneREN
is asnp
is mentioned by
dbSNPrs121917743
ebirs121917743
HLIrs121917743
Exacrs121917743
Varsomers121917743
Maprs121917743
PheGenIrs121917743
hapmaprs121917743
1000 genomesrs121917743
hgdprs121917743
ensemblrs121917743
gopubmedrs121917743
geneviewrs121917743
scholarrs121917743
googlers121917743
pharmgkbrs121917743
gwascentralrs121917743
openSNPrs121917743
23andMers121917743
23andMe allrs121917743
SNP Nexus

SNPshotrs121917743
SNPdbers121917743
MSV3drs121917743
GWAS Ctlgrs121917743
Max Magnitude0
OMIM179820
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121917743(G;G)
Alt rs121917743(G;G)
Reference rs121917743(T;T)
Significance Pathogenic
Disease Hyperuricemic nephropathy
Variation info
Gene REN
CLNDBN Hyperuricemic nephropathy, familial juvenile, 2
Reversed 1
HGVS NC_000001.10:g.204135375A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000014006.23,