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rs273585650

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs273585650(G;G)
Make rs273585650(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position50090220
GeneCLCN5
is asnp
is mentioned by
dbSNPrs273585650
ebirs273585650
HLIrs273585650
Exacrs273585650
Varsomers273585650
Maprs273585650
PheGenIrs273585650
hapmaprs273585650
1000 genomesrs273585650
hgdprs273585650
ensemblrs273585650
gopubmedrs273585650
geneviewrs273585650
scholarrs273585650
googlers273585650
pharmgkbrs273585650
gwascentralrs273585650
openSNPrs273585650
23andMers273585650
23andMe allrs273585650
SNP Nexus

SNPshotrs273585650
SNPdbers273585650
MSV3drs273585650
GWAS Ctlgrs273585650
Max Magnitude0
ClinVar
Risk rs273585650(G;G)
Alt rs273585650(G;G)
Reference rs273585650(T;T)
Significance Pathogenic
Disease Dent disease 1
Variation info
Gene CLCN5
CLNDBN Dent disease 1
Reversed 0
HGVS NC_000023.10:g.49854877T>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000033875.2,