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rs797044809

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044809(A;A)
Make rs797044809(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position50086359
GeneCLCN5
is asnp
is mentioned by
dbSNPrs797044809
ebirs797044809
HLIrs797044809
Exacrs797044809
Varsomers797044809
Maprs797044809
PheGenIrs797044809
hapmaprs797044809
1000 genomesrs797044809
hgdprs797044809
ensemblrs797044809
gopubmedrs797044809
geneviewrs797044809
scholarrs797044809
googlers797044809
pharmgkbrs797044809
gwascentralrs797044809
openSNPrs797044809
23andMers797044809
23andMe allrs797044809
SNP Nexus

SNPshotrs797044809
SNPdbers797044809
MSV3drs797044809
GWAS Ctlgrs797044809
Max Magnitude0
ClinVar
Risk rs797044809(A;A)
Alt rs797044809(A;A)
Reference rs797044809(G;G)
Significance Pathogenic
Disease Dent disease 1
Variation info
Gene CLCN5
CLNDBN Dent disease 1
Reversed 0
HGVS NC_000023.10:g.49851016G>A
CLNSRC
CLNACC RCV000192275.1,