rs137852691

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs137852691(C;G)

Make rs137852691(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

132657203

Gene

OPCML

is a	snp
is	mentioned by
dbSNP	rs137852691
dbSNP (classic)	rs137852691
ClinGen	rs137852691
ebi	rs137852691
HLI	rs137852691
Exac	rs137852691
Gnomad	rs137852691
Varsome	rs137852691
LitVar	rs137852691
Map	rs137852691
PheGenI	rs137852691
Biobank	rs137852691
1000 genomes	rs137852691
hgdp	rs137852691
ensembl	rs137852691
geneview	rs137852691
scholar	rs137852691
google	rs137852691
pharmgkb	rs137852691
gwascentral	rs137852691
openSNP	rs137852691
23andMe	rs137852691
SNPshot	rs137852691
SNPdbe	rs137852691
MSV3d	rs137852691
GWAS Ctlg	rs137852691

Max Magnitude

0

OMIM	600632
Desc
Variant	0001
Related	also

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,