rs786202517

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(AC;GG)	6.3	Hereditary cancer predisposing syndrome
(GG;GG)	0	common in clinvar

Make rs786202517(AC;AC)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

87894050

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs786202517
dbSNP (classic)	rs786202517
ClinGen	rs786202517
ebi	rs786202517
HLI	rs786202517
Exac	rs786202517
Gnomad	rs786202517
Varsome	rs786202517
LitVar	rs786202517
Map	rs786202517
PheGenI	rs786202517
Biobank	rs786202517
1000 genomes	rs786202517
hgdp	rs786202517
ensembl	rs786202517
geneview	rs786202517
scholar	rs786202517
google	rs786202517
pharmgkb	rs786202517
gwascentral	rs786202517
openSNP	rs786202517
23andMe	rs786202517
SNPshot	rs786202517
SNPdbe	rs786202517
MSV3d	rs786202517
GWAS Ctlg	rs786202517

Max Magnitude

6.3

ClinVar
Risk	rs786202517(AC;AC)
Alt	rs786202517(AC;AC)
Reference	Rs786202517(GG;GG)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89653807_89653808delGGinsAC
CLNSRC
CLNACC	RCV000165361.1,