rs587782350

Orientation

plus

Stabilized

plus

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

Make rs587782350(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

10

Position

87957955

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs587782350
dbSNP (classic)	rs587782350
ClinGen	rs587782350
ebi	rs587782350
HLI	rs587782350
Exac	rs587782350
Gnomad	rs587782350
Varsome	rs587782350
LitVar	rs587782350
Map	rs587782350
PheGenI	rs587782350
Biobank	rs587782350
1000 genomes	rs587782350
hgdp	rs587782350
ensembl	rs587782350
geneview	rs587782350
scholar	rs587782350
google	rs587782350
pharmgkb	rs587782350
gwascentral	rs587782350
openSNP	rs587782350
23andMe	rs587782350
SNPshot	rs587782350
SNPdbe	rs587782350
MSV3d	rs587782350
GWAS Ctlg	rs587782350

Max Magnitude

6.3

ClinVar
Risk	rs587782350(T;T)
Alt	rs587782350(T;T)
Reference	Rs587782350(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000010.10:g.89717712C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000131292.4, RCV000212883.1,