rs876660535

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;G)	6.3	Cowden syndrome (PTEN hamartoma tumor syndrome)
(G;G)	0	common in clinvar

Make rs876660535(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

10

Position

87933130

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs876660535
dbSNP (classic)	rs876660535
ClinGen	rs876660535
ebi	rs876660535
HLI	rs876660535
Exac	rs876660535
Gnomad	rs876660535
Varsome	rs876660535
LitVar	rs876660535
Map	rs876660535
PheGenI	rs876660535
Biobank	rs876660535
1000 genomes	rs876660535
hgdp	rs876660535
ensembl	rs876660535
geneview	rs876660535
scholar	rs876660535
google	rs876660535
pharmgkb	rs876660535
gwascentral	rs876660535
openSNP	rs876660535
23andMe	rs876660535
SNPshot	rs876660535
SNPdbe	rs876660535
MSV3d	rs876660535
GWAS Ctlg	rs876660535

Max Magnitude

6.3

ClinVar
Risk	rs876660535(A;A)
Alt	rs876660535(A;A)
Reference	Rs876660535(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome PTEN hamartoma tumor syndrome
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome PTEN hamartoma tumor syndrome
Reversed	0
HGVS	NC_000010.10:g.89692887G>A
CLNSRC
CLNACC	RCV000220547.2, RCV000471590.1,