rs876660634

Orientation

plus

Stabilized

plus

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

Make rs876660634(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

10

Position

87925551

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs876660634
dbSNP (classic)	rs876660634
ClinGen	rs876660634
ebi	rs876660634
HLI	rs876660634
Exac	rs876660634
Gnomad	rs876660634
Varsome	rs876660634
LitVar	rs876660634
Map	rs876660634
PheGenI	rs876660634
Biobank	rs876660634
1000 genomes	rs876660634
hgdp	rs876660634
ensembl	rs876660634
geneview	rs876660634
scholar	rs876660634
google	rs876660634
pharmgkb	rs876660634
gwascentral	rs876660634
openSNP	rs876660634
23andMe	rs876660634
SNPshot	rs876660634
SNPdbe	rs876660634
MSV3d	rs876660634
GWAS Ctlg	rs876660634

Max Magnitude

6.3

ClinVar
Risk	rs876660634(G;G)
Alt	rs876660634(G;G)
Reference	Rs876660634(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89685308A>G
CLNSRC
CLNACC	RCV000215167.1,