rs786204933

Orientation

plus

Stabilized

plus

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

Make rs786204933(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

87933196

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs786204933
dbSNP (classic)	rs786204933
ClinGen	rs786204933
ebi	rs786204933
HLI	rs786204933
Exac	rs786204933
Gnomad	rs786204933
Varsome	rs786204933
LitVar	rs786204933
Map	rs786204933
PheGenI	rs786204933
Biobank	rs786204933
1000 genomes	rs786204933
hgdp	rs786204933
ensembl	rs786204933
geneview	rs786204933
scholar	rs786204933
google	rs786204933
pharmgkb	rs786204933
gwascentral	rs786204933
openSNP	rs786204933
23andMe	rs786204933
SNPshot	rs786204933
SNPdbe	rs786204933
MSV3d	rs786204933
GWAS Ctlg	rs786204933

Max Magnitude

6.3

ClinVar
Risk	rs786204933(A;A) rs786204933(G;G)
Alt	rs786204933(A;A) rs786204933(G;G)
Reference	Rs786204933(T;T)
Significance	Pathogenic
Disease	not provided PTEN hamartoma tumor syndrome
Variation	info
Gene	PTEN
CLNDBN	not provided PTEN hamartoma tumor syndrome
Reversed	0
HGVS	NC_000010.10:g.89692953T>A; NC_000010.10:g.89692953T>G
CLNSRC
CLNACC	RCV000169878.1, RCV000198975.2,