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rs151340628

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151340628(C;C)
Make rs151340628(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position50086362
GeneCLCN5
is asnp
is mentioned by
dbSNPrs151340628
ebirs151340628
HLIrs151340628
Exacrs151340628
Varsomers151340628
Maprs151340628
PheGenIrs151340628
hapmaprs151340628
1000 genomesrs151340628
hgdprs151340628
ensemblrs151340628
gopubmedrs151340628
geneviewrs151340628
scholarrs151340628
googlers151340628
pharmgkbrs151340628
gwascentralrs151340628
openSNPrs151340628
23andMers151340628
23andMe allrs151340628
SNP Nexus

SNPshotrs151340628
SNPdbers151340628
MSV3drs151340628
GWAS Ctlgrs151340628
Max Magnitude0
ClinVar
Risk rs151340628(A,C;A,C)
Alt rs151340628(A,C;A,C)
Reference rs151340628(G;G)
Significance Pathogenic
Disease Proteinuria
Variation info
Gene CLCN5
CLNDBN Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis
Reversed 0
HGVS NC_000023.10:g.49851019G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000012573.16,