rs786202840

Orientation

plus

Stabilized

plus

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

Make rs786202840(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

87960942

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs786202840
dbSNP (classic)	rs786202840
ClinGen	rs786202840
ebi	rs786202840
HLI	rs786202840
Exac	rs786202840
Gnomad	rs786202840
Varsome	rs786202840
LitVar	rs786202840
Map	rs786202840
PheGenI	rs786202840
Biobank	rs786202840
1000 genomes	rs786202840
hgdp	rs786202840
ensembl	rs786202840
geneview	rs786202840
scholar	rs786202840
google	rs786202840
pharmgkb	rs786202840
gwascentral	rs786202840
openSNP	rs786202840
23andMe	rs786202840
SNPshot	rs786202840
SNPdbe	rs786202840
MSV3d	rs786202840
GWAS Ctlg	rs786202840

Max Magnitude

6.3

ClinVar
Risk	rs786202840(T;T)
Alt	rs786202840(T;T)
Reference	Rs786202840(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.89720699G>T
CLNSRC
CLNACC	RCV000165862.1,