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rs137853846

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853846(C;T)
Make rs137853846(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position129569274
GeneOCRL
is asnp
is mentioned by
dbSNPrs137853846
ebirs137853846
HLIrs137853846
Exacrs137853846
Varsomers137853846
Maprs137853846
PheGenIrs137853846
hapmaprs137853846
1000 genomesrs137853846
hgdprs137853846
ensemblrs137853846
gopubmedrs137853846
geneviewrs137853846
scholarrs137853846
googlers137853846
pharmgkbrs137853846
gwascentralrs137853846
openSNPrs137853846
23andMers137853846
23andMe allrs137853846
SNP Nexus

SNPshotrs137853846
SNPdbers137853846
MSV3drs137853846
GWAS Ctlgrs137853846
Max Magnitude0
ClinVar
Risk rs137853846(T;T)
Alt rs137853846(T;T)
Reference rs137853846(C;C)
Significance Probable-Pathogenic
Disease Dent disease 2
Variation info
Gene OCRL
CLNDBN Dent disease 2
Reversed 0
HGVS NC_000023.10:g.128703251C>T
CLNSRC UniProtKB (variants)
CLNACC RCV000059593.2,