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rs273585646

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs273585646(A;A)
Make rs273585646(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position50086543
GeneCLCN5
is asnp
is mentioned by
dbSNPrs273585646
ebirs273585646
HLIrs273585646
Exacrs273585646
Varsomers273585646
Maprs273585646
PheGenIrs273585646
hapmaprs273585646
1000 genomesrs273585646
hgdprs273585646
ensemblrs273585646
gopubmedrs273585646
geneviewrs273585646
scholarrs273585646
googlers273585646
pharmgkbrs273585646
gwascentralrs273585646
openSNPrs273585646
23andMers273585646
23andMe allrs273585646
SNP Nexus

SNPshotrs273585646
SNPdbers273585646
MSV3drs273585646
GWAS Ctlgrs273585646
Max Magnitude0
ClinVar
Risk rs273585646(A;A)
Alt rs273585646(A;A)
Reference rs273585646(C;C)
Significance Pathogenic
Disease Dent disease 1
Variation info
Gene CLCN5
CLNDBN Dent disease 1
Reversed 0
HGVS NC_000023.10:g.49851200C>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000033872.2,