rs587780005

Orientation

plus

Stabilized

plus

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

Make rs587780005(G;G)

Make rs587780005(G;T)

Reference

GRCh38.p2 38.2/144

Chromosome

10

Position

87925541

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs587780005
dbSNP (classic)	rs587780005
ClinGen	rs587780005
ebi	rs587780005
HLI	rs587780005
Exac	rs587780005
Gnomad	rs587780005
Varsome	rs587780005
LitVar	rs587780005
Map	rs587780005
PheGenI	rs587780005
Biobank	rs587780005
1000 genomes	rs587780005
hgdp	rs587780005
ensembl	rs587780005
geneview	rs587780005
scholar	rs587780005
google	rs587780005
pharmgkb	rs587780005
gwascentral	rs587780005
openSNP	rs587780005
23andMe	rs587780005
SNPshot	rs587780005
SNPdbe	rs587780005
MSV3d	rs587780005
GWAS Ctlg	rs587780005

Max Magnitude

0

ClinVar
Risk	rs587780005(G;G)
Alt	rs587780005(G;G)
Reference	Rs587780005(T;T)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89685298T>G
CLNSRC
CLNACC	RCV000115584.2,