rs587782603

Orientation

plus

Stabilized

plus

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

Make rs587782603(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

10

Position

87952118

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs587782603
dbSNP (classic)	rs587782603
ClinGen	rs587782603
ebi	rs587782603
HLI	rs587782603
Exac	rs587782603
Gnomad	rs587782603
Varsome	rs587782603
LitVar	rs587782603
Map	rs587782603
PheGenI	rs587782603
Biobank	rs587782603
1000 genomes	rs587782603
hgdp	rs587782603
ensembl	rs587782603
geneview	rs587782603
scholar	rs587782603
google	rs587782603
pharmgkb	rs587782603
gwascentral	rs587782603
openSNP	rs587782603
23andMe	rs587782603
SNPshot	rs587782603
SNPdbe	rs587782603
MSV3d	rs587782603
GWAS Ctlg	rs587782603

Max Magnitude

6.3

ClinVar
Risk	rs587782603(A;A) rs587782603(T;T)
Alt	rs587782603(A;A) rs587782603(T;T)
Reference	Rs587782603(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.89711875G>A; NC_000010.10:g.89711875G>T
CLNSRC
CLNACC	RCV000491530.1, RCV000131967.2,