rs587776667

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;G)	6.3	Endometrial carcinoma (indicated)
(G;G)	0	common in clinvar
(G;T)	6.3	Hereditary cancer predisposing syndrome

Make rs587776667(A;A)

Reference

GRCh38 38.1/142

Chromosome

10

Position

87931090

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs587776667
dbSNP (classic)	rs587776667
ClinGen	rs587776667
ebi	rs587776667
HLI	rs587776667
Exac	rs587776667
Gnomad	rs587776667
Varsome	rs587776667
LitVar	rs587776667
Map	rs587776667
PheGenI	rs587776667
Biobank	rs587776667
1000 genomes	rs587776667
hgdp	rs587776667
ensembl	rs587776667
geneview	rs587776667
scholar	rs587776667
google	rs587776667
pharmgkb	rs587776667
gwascentral	rs587776667
openSNP	rs587776667
23andMe	rs587776667
SNPshot	rs587776667
SNPdbe	rs587776667
MSV3d	rs587776667
GWAS Ctlg	rs587776667

Max Magnitude

6.3

ClinVar
Risk	rs587776667(A;A) rs587776667(C;C) rs587776667(T;T)
Alt	rs587776667(A;A) rs587776667(C;C) rs587776667(T;T)
Reference	Rs587776667(G;G)
Significance	Pathogenic
Disease	Endometrial carcinoma not provided PTEN hamartoma tumor syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN
CLNDBN	Endometrial carcinoma not provided PTEN hamartoma tumor syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89690847G>A; NC_000010.10:g.89690847G>C; NC_000010.10:g.89690847G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008266.3, RCV000433259.1, RCV000490594.1, RCV000491885.1, RCV000169865.2,