rs786202733

Orientation

plus

Stabilized

plus

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

Make rs786202733(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

87952165

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs786202733
dbSNP (classic)	rs786202733
ClinGen	rs786202733
ebi	rs786202733
HLI	rs786202733
Exac	rs786202733
Gnomad	rs786202733
Varsome	rs786202733
LitVar	rs786202733
Map	rs786202733
PheGenI	rs786202733
Biobank	rs786202733
1000 genomes	rs786202733
hgdp	rs786202733
ensembl	rs786202733
geneview	rs786202733
scholar	rs786202733
google	rs786202733
pharmgkb	rs786202733
gwascentral	rs786202733
openSNP	rs786202733
23andMe	rs786202733
SNPshot	rs786202733
SNPdbe	rs786202733
MSV3d	rs786202733
GWAS Ctlg	rs786202733

Max Magnitude

6.3

ClinVar
Risk	rs786202733(G;G)
Alt	rs786202733(G;G)
Reference	Rs786202733(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89711922C>G
CLNSRC
CLNACC	RCV000165694.1,