rs587782345

Orientation

plus

Stabilized

plus

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

Make rs587782345(A;G)

Make rs587782345(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

10

Position

87965326

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs587782345
dbSNP (classic)	rs587782345
ClinGen	rs587782345
ebi	rs587782345
HLI	rs587782345
Exac	rs587782345
Gnomad	rs587782345
Varsome	rs587782345
LitVar	rs587782345
Map	rs587782345
PheGenI	rs587782345
Biobank	rs587782345
1000 genomes	rs587782345
hgdp	rs587782345
ensembl	rs587782345
geneview	rs587782345
scholar	rs587782345
google	rs587782345
pharmgkb	rs587782345
gwascentral	rs587782345
openSNP	rs587782345
23andMe	rs587782345
SNPshot	rs587782345
SNPdbe	rs587782345
MSV3d	rs587782345
GWAS Ctlg	rs587782345

Max Magnitude

0

ClinVar
Risk	rs587782345(C;C) rs587782345(G;G) rs587782345(T;T)
Alt	rs587782345(C;C) rs587782345(G;G) rs587782345(T;T)
Reference	Rs587782345(A;A)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome PTEN hamartoma tumor syndrome not specified
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome PTEN hamartoma tumor syndrome not specified
Reversed	0
HGVS	NC_000010.10:g.89725083A>G; NC_000010.10:g.89725083A>T
CLNSRC
CLNACC	RCV000131284.2, RCV000463640.1, RCV000169786.2, RCV000456755.1,