rs1085308056

Orientation

plus

Stabilized

plus

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

Chromosome

10

Position

87957850

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs1085308056
dbSNP (classic)	rs1085308056
ClinGen	rs1085308056
ebi	rs1085308056
HLI	rs1085308056
Exac	rs1085308056
Gnomad	rs1085308056
Varsome	rs1085308056
LitVar	rs1085308056
Map	rs1085308056
PheGenI	rs1085308056
Biobank	rs1085308056
1000 genomes	rs1085308056
hgdp	rs1085308056
ensembl	rs1085308056
geneview	rs1085308056
scholar	rs1085308056
google	rs1085308056
pharmgkb	rs1085308056
gwascentral	rs1085308056
openSNP	rs1085308056
23andMe	rs1085308056
SNPshot	rs1085308056
SNPdbe	rs1085308056
MSV3d	rs1085308056
GWAS Ctlg	rs1085308056

Max Magnitude

0

ClinVar
Risk	rs1085308056(G;G)
Alt	rs1085308056(G;G)
Reference	Rs1085308056(C;C)
Significance	Pathogenic
Disease	PTEN hamartoma tumor syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN
CLNDBN	PTEN hamartoma tumor syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89717607C>G
CLNSRC
CLNACC	RCV000490589.1, RCV000491647.1,