rs786204905

Orientation

plus

Stabilized

plus

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

Make rs786204905(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

87960967

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs786204905
dbSNP (classic)	rs786204905
ClinGen	rs786204905
ebi	rs786204905
HLI	rs786204905
Exac	rs786204905
Gnomad	rs786204905
Varsome	rs786204905
LitVar	rs786204905
Map	rs786204905
PheGenI	rs786204905
Biobank	rs786204905
1000 genomes	rs786204905
hgdp	rs786204905
ensembl	rs786204905
geneview	rs786204905
scholar	rs786204905
google	rs786204905
pharmgkb	rs786204905
gwascentral	rs786204905
openSNP	rs786204905
23andMe	rs786204905
SNPshot	rs786204905
SNPdbe	rs786204905
MSV3d	rs786204905
GWAS Ctlg	rs786204905

Max Magnitude

6.3

ClinVar
Risk	rs786204905(A;A)
Alt	rs786204905(A;A)
Reference	Rs786204905(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89720724dupA
CLNSRC
CLNACC	RCV000169846.1,