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rs151340625

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151340625(A;A)
Make rs151340625(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position50088867
GeneCLCN5
is asnp
is mentioned by
dbSNPrs151340625
ebirs151340625
HLIrs151340625
Exacrs151340625
Varsomers151340625
Maprs151340625
PheGenIrs151340625
hapmaprs151340625
1000 genomesrs151340625
hgdprs151340625
ensemblrs151340625
gopubmedrs151340625
geneviewrs151340625
scholarrs151340625
googlers151340625
pharmgkbrs151340625
gwascentralrs151340625
openSNPrs151340625
23andMers151340625
23andMe allrs151340625
SNP Nexus

SNPshotrs151340625
SNPdbers151340625
MSV3drs151340625
GWAS Ctlgrs151340625
Max Magnitude0
ClinVar
Risk rs151340625(A;A)
Alt rs151340625(A;A)
Reference rs151340625(G;G)
Significance Pathogenic
Disease Nephrolithiasis
Variation info
Gene CLCN5
CLNDBN Nephrolithiasis, X-linked recessive
Reversed 0
HGVS NC_000023.10:g.49853524G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012569.14,