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rs151340621

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151340621(C;T)
Make rs151340621(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position50090678
GeneCLCN5
is asnp
is mentioned by
dbSNPrs151340621
ClinGenrs151340621
ebirs151340621
HLIrs151340621
Exacrs151340621
Varsomers151340621
Maprs151340621
PheGenIrs151340621
hapmaprs151340621
1000 genomesrs151340621
hgdprs151340621
ensemblrs151340621
gopubmedrs151340621
geneviewrs151340621
scholarrs151340621
googlers151340621
pharmgkbrs151340621
gwascentralrs151340621
openSNPrs151340621
23andMers151340621
23andMe allrs151340621
SNP Nexus

SNPshotrs151340621
SNPdbers151340621
MSV3drs151340621
GWAS Ctlgrs151340621
Max Magnitude0
ClinVar
Risk rs151340621(A;A) rs151340621(T;T)
Alt rs151340621(A;A) rs151340621(T;T)
Reference Rs151340621(C;C)
Significance Pathogenic
Disease Dent disease 1
Variation info
Gene CLCN5
CLNDBN Dent disease 1
Reversed 0
HGVS NC_000023.10:g.49855335C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012565.16,