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rs273585647

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs273585647(A;A)
Make rs273585647(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position50090118
GeneCLCN5
is asnp
is mentioned by
dbSNPrs273585647
ebirs273585647
HLIrs273585647
Exacrs273585647
Varsomers273585647
Maprs273585647
PheGenIrs273585647
hapmaprs273585647
1000 genomesrs273585647
hgdprs273585647
ensemblrs273585647
gopubmedrs273585647
geneviewrs273585647
scholarrs273585647
googlers273585647
pharmgkbrs273585647
gwascentralrs273585647
openSNPrs273585647
23andMers273585647
23andMe allrs273585647
SNP Nexus

SNPshotrs273585647
SNPdbers273585647
MSV3drs273585647
GWAS Ctlgrs273585647
Max Magnitude0
ClinVar
Risk rs273585647(A;A)
Alt rs273585647(A;A)
Reference rs273585647(G;G)
Significance Pathogenic
Disease Dent disease 1
Variation info
Gene CLCN5
CLNDBN Dent disease 1
Reversed 0
HGVS NC_000023.10:g.49854775G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000033873.2,