rs876658837

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;G)	6.3	Hereditary cancer predisposing syndrome
(G;G)	0	common in clinvar

Make rs876658837(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

10

Position

87961041

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs876658837
dbSNP (classic)	rs876658837
ClinGen	rs876658837
ebi	rs876658837
HLI	rs876658837
Exac	rs876658837
Gnomad	rs876658837
Varsome	rs876658837
LitVar	rs876658837
Map	rs876658837
PheGenI	rs876658837
Biobank	rs876658837
1000 genomes	rs876658837
hgdp	rs876658837
ensembl	rs876658837
geneview	rs876658837
scholar	rs876658837
google	rs876658837
pharmgkb	rs876658837
gwascentral	rs876658837
openSNP	rs876658837
23andMe	rs876658837
SNPshot	rs876658837
SNPdbe	rs876658837
MSV3d	rs876658837
GWAS Ctlg	rs876658837

Max Magnitude

6.3

ClinVar
Risk	rs876658837(-;-)
Alt	rs876658837(-;-)
Reference	Rs876658837(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89720798delG
CLNSRC
CLNACC	RCV000217505.1,