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rs151340620

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151340620(A;A)
Make rs151340620(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position50086360
GeneCLCN5
is asnp
is mentioned by
dbSNPrs151340620
ebirs151340620
HLIrs151340620
Exacrs151340620
Varsomers151340620
Maprs151340620
PheGenIrs151340620
hapmaprs151340620
1000 genomesrs151340620
hgdprs151340620
ensemblrs151340620
gopubmedrs151340620
geneviewrs151340620
scholarrs151340620
googlers151340620
pharmgkbrs151340620
gwascentralrs151340620
openSNPrs151340620
23andMers151340620
23andMe allrs151340620
SNP Nexus

SNPshotrs151340620
SNPdbers151340620
MSV3drs151340620
GWAS Ctlgrs151340620
Max Magnitude0
ClinVar
Risk rs151340620(A;A)
Alt rs151340620(A;A)
Reference rs151340620(G;G)
Significance Pathogenic
Disease Dent disease 1 Proteinuria
Variation info
Gene CLCN5
CLNDBN Dent disease 1 Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis
Reversed 0
HGVS NC_000023.10:g.49851017G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012563.14, RCV000012564.24,