rs587782607

Orientation

plus

Stabilized

plus

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

Make rs587782607(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

10

Position

87960914

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs587782607
dbSNP (classic)	rs587782607
ClinGen	rs587782607
ebi	rs587782607
HLI	rs587782607
Exac	rs587782607
Gnomad	rs587782607
Varsome	rs587782607
LitVar	rs587782607
Map	rs587782607
PheGenI	rs587782607
Biobank	rs587782607
1000 genomes	rs587782607
hgdp	rs587782607
ensembl	rs587782607
geneview	rs587782607
scholar	rs587782607
google	rs587782607
pharmgkb	rs587782607
gwascentral	rs587782607
openSNP	rs587782607
23andMe	rs587782607
SNPshot	rs587782607
SNPdbe	rs587782607
MSV3d	rs587782607
GWAS Ctlg	rs587782607

Max Magnitude

6.3

ClinVar
Risk	rs587782607(A;A)
Alt	rs587782607(A;A)
Reference	Rs587782607(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.89720671G>A
CLNSRC
CLNACC	RCV000131976.2,