rs876661024

Orientation

plus

Stabilized

plus

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

Make rs876661024(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

10

Position

87957852

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs876661024
dbSNP (classic)	rs876661024
ClinGen	rs876661024
ebi	rs876661024
HLI	rs876661024
Exac	rs876661024
Gnomad	rs876661024
Varsome	rs876661024
LitVar	rs876661024
Map	rs876661024
PheGenI	rs876661024
Biobank	rs876661024
1000 genomes	rs876661024
hgdp	rs876661024
ensembl	rs876661024
geneview	rs876661024
scholar	rs876661024
google	rs876661024
pharmgkb	rs876661024
gwascentral	rs876661024
openSNP	rs876661024
23andMe	rs876661024
SNPshot	rs876661024
SNPdbe	rs876661024
MSV3d	rs876661024
GWAS Ctlg	rs876661024

Max Magnitude

6.3

ClinVar
Risk	rs876661024(A;A) rs876661024(C;C)
Alt	rs876661024(A;A) rs876661024(C;C)
Reference	Rs876661024(G;G)
Significance	Pathogenic
Disease	PTEN hamartoma tumor syndrome not provided
Variation	info
Gene	PTEN
CLNDBN	PTEN hamartoma tumor syndrome not provided
Reversed	0
HGVS	NC_000010.10:g.89717609G>A; NC_000010.10:g.89717609G>C
CLNSRC
CLNACC	RCV000490578.1, RCV000221132.1,