Have questions? Visit https://www.reddit.com/r/SNPedia

rs273585648

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs273585648(C;C)
Make rs273585648(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position50086357
GeneCLCN5
is asnp
is mentioned by
dbSNPrs273585648
ebirs273585648
HLIrs273585648
Exacrs273585648
Varsomers273585648
Maprs273585648
PheGenIrs273585648
hapmaprs273585648
1000 genomesrs273585648
hgdprs273585648
ensemblrs273585648
gopubmedrs273585648
geneviewrs273585648
scholarrs273585648
googlers273585648
pharmgkbrs273585648
gwascentralrs273585648
openSNPrs273585648
23andMers273585648
23andMe allrs273585648
SNP Nexus

SNPshotrs273585648
SNPdbers273585648
MSV3drs273585648
GWAS Ctlgrs273585648
Max Magnitude0
ClinVar
Risk rs273585648(C;C)
Alt rs273585648(C;C)
Reference rs273585648(G;G)
Significance Pathogenic
Disease Dent disease 1
Variation info
Gene CLCN5
CLNDBN Dent disease 1
Reversed 0
HGVS NC_000023.10:g.49851014G>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000033878.2,