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rs137852691

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852691(C;G)
Make rs137852691(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position132657203
GeneOPCML
is asnp
is mentioned by
dbSNPrs137852691
ebirs137852691
HLIrs137852691
Exacrs137852691
Varsomers137852691
Maprs137852691
PheGenIrs137852691
hapmaprs137852691
1000 genomesrs137852691
hgdprs137852691
ensemblrs137852691
gopubmedrs137852691
geneviewrs137852691
scholarrs137852691
googlers137852691
pharmgkbrs137852691
gwascentralrs137852691
openSNPrs137852691
23andMers137852691
23andMe allrs137852691
SNP Nexus

SNPshotrs137852691
SNPdbers137852691
MSV3drs137852691
GWAS Ctlgrs137852691
Max Magnitude0
OMIM600632
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137852691(G;G)
Alt rs137852691(G;G)
Reference rs137852691(C;C)
Significance Pathogenic
Disease Neoplasm of ovary
Variation info
Gene OPCML
CLNDBN Neoplasm of ovary
Reversed 1
HGVS NC_000011.9:g.132527098G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000009546.4,