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rs273585644

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs273585644(A;G)
Make rs273585644(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position50086338
GeneCLCN5
is asnp
is mentioned by
dbSNPrs273585644
ebirs273585644
HLIrs273585644
Exacrs273585644
Varsomers273585644
Maprs273585644
PheGenIrs273585644
hapmaprs273585644
1000 genomesrs273585644
hgdprs273585644
ensemblrs273585644
gopubmedrs273585644
geneviewrs273585644
scholarrs273585644
googlers273585644
pharmgkbrs273585644
gwascentralrs273585644
openSNPrs273585644
23andMers273585644
23andMe allrs273585644
SNP Nexus

SNPshotrs273585644
SNPdbers273585644
MSV3drs273585644
GWAS Ctlgrs273585644
Max Magnitude0
ClinVar
Risk rs273585644(G;G)
Alt rs273585644(G;G)
Reference rs273585644(A;A)
Significance Pathogenic
Disease Dent disease 1
Variation info
Gene CLCN5
CLNDBN Dent disease 1
Reversed 0
HGVS NC_000023.10:g.49850995A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000033877.2,