rs786204859

Orientation

plus

Stabilized

plus

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

Make rs786204859(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

87933166

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs786204859
dbSNP (classic)	rs786204859
ClinGen	rs786204859
ebi	rs786204859
HLI	rs786204859
Exac	rs786204859
Gnomad	rs786204859
Varsome	rs786204859
LitVar	rs786204859
Map	rs786204859
PheGenI	rs786204859
Biobank	rs786204859
1000 genomes	rs786204859
hgdp	rs786204859
ensembl	rs786204859
geneview	rs786204859
scholar	rs786204859
google	rs786204859
pharmgkb	rs786204859
gwascentral	rs786204859
openSNP	rs786204859
23andMe	rs786204859
SNPshot	rs786204859
SNPdbe	rs786204859
MSV3d	rs786204859
GWAS Ctlg	rs786204859

Max Magnitude

6.3

ClinVar
Risk	rs786204859(A;A)
Alt	rs786204859(A;A)
Reference	Rs786204859(G;G)
Significance	Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN
CLNDBN	not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89692923G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000169797.2, RCV000217011.2,