rs786202529

Orientation

plus

Stabilized

plus

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

Make rs786202529(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

87957924

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs786202529
dbSNP (classic)	rs786202529
ClinGen	rs786202529
ebi	rs786202529
HLI	rs786202529
Exac	rs786202529
Gnomad	rs786202529
Varsome	rs786202529
LitVar	rs786202529
Map	rs786202529
PheGenI	rs786202529
Biobank	rs786202529
1000 genomes	rs786202529
hgdp	rs786202529
ensembl	rs786202529
geneview	rs786202529
scholar	rs786202529
google	rs786202529
pharmgkb	rs786202529
gwascentral	rs786202529
openSNP	rs786202529
23andMe	rs786202529
SNPshot	rs786202529
SNPdbe	rs786202529
MSV3d	rs786202529
GWAS Ctlg	rs786202529

Max Magnitude

6.3

ClinVar
Risk	rs786202529(G;G)
Alt	rs786202529(G;G)
Reference	Rs786202529(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89717681dupG
CLNSRC
CLNACC	RCV000165377.1,