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rs273585649

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs273585649(A;G)
Make rs273585649(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position50090218
GeneCLCN5
is asnp
is mentioned by
dbSNPrs273585649
ebirs273585649
HLIrs273585649
Exacrs273585649
Varsomers273585649
Maprs273585649
PheGenIrs273585649
hapmaprs273585649
1000 genomesrs273585649
hgdprs273585649
ensemblrs273585649
gopubmedrs273585649
geneviewrs273585649
scholarrs273585649
googlers273585649
pharmgkbrs273585649
gwascentralrs273585649
openSNPrs273585649
23andMers273585649
23andMe allrs273585649
SNP Nexus

SNPshotrs273585649
SNPdbers273585649
MSV3drs273585649
GWAS Ctlgrs273585649
Max Magnitude0
ClinVar
Risk rs273585649(G;G)
Alt rs273585649(G;G)
Reference rs273585649(A;A)
Significance Pathogenic
Disease Dent disease 1
Variation info
Gene CLCN5
CLNDBN Dent disease 1
Reversed 0
HGVS NC_000023.10:g.49854875A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000033874.2,