rs876661058

Orientation

plus

Stabilized

plus

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

Make rs876661058(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

10

Position

87961037

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs876661058
dbSNP (classic)	rs876661058
ClinGen	rs876661058
ebi	rs876661058
HLI	rs876661058
Exac	rs876661058
Gnomad	rs876661058
Varsome	rs876661058
LitVar	rs876661058
Map	rs876661058
PheGenI	rs876661058
Biobank	rs876661058
1000 genomes	rs876661058
hgdp	rs876661058
ensembl	rs876661058
geneview	rs876661058
scholar	rs876661058
google	rs876661058
pharmgkb	rs876661058
gwascentral	rs876661058
openSNP	rs876661058
23andMe	rs876661058
SNPshot	rs876661058
SNPdbe	rs876661058
MSV3d	rs876661058
GWAS Ctlg	rs876661058

Max Magnitude

6.3

ClinVar
Risk	rs876661058(A;A) rs876661058(G;G)
Alt	rs876661058(A;A) rs876661058(G;G)
Reference	Rs876661058(T;T)
Significance	Pathogenic
Disease	not provided PTEN hamartoma tumor syndrome
Variation	info
Gene	PTEN
CLNDBN	not provided PTEN hamartoma tumor syndrome
Reversed	0
HGVS	NC_000010.10:g.89720794T>A; NC_000010.10:g.89720794T>G
CLNSRC
CLNACC	RCV000222109.1, RCV000475538.1,