rs786204934

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar
(G;T)	6.3	Cowden syndrome (PTEN hamartoma tumor syndrome)

Make rs786204934(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

87933207

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs786204934
dbSNP (classic)	rs786204934
ClinGen	rs786204934
ebi	rs786204934
HLI	rs786204934
Exac	rs786204934
Gnomad	rs786204934
Varsome	rs786204934
LitVar	rs786204934
Map	rs786204934
PheGenI	rs786204934
Biobank	rs786204934
1000 genomes	rs786204934
hgdp	rs786204934
ensembl	rs786204934
geneview	rs786204934
scholar	rs786204934
google	rs786204934
pharmgkb	rs786204934
gwascentral	rs786204934
openSNP	rs786204934
23andMe	rs786204934
SNPshot	rs786204934
SNPdbe	rs786204934
MSV3d	rs786204934
GWAS Ctlg	rs786204934

Max Magnitude

6.3

ClinVar
Risk	rs786204934(T;T)
Alt	rs786204934(T;T)
Reference	Rs786204934(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89692964G>T
CLNSRC
CLNACC	RCV000491120.1,