rs876659456

Orientation

plus

Stabilized

plus

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

Make rs876659456(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

10

Position

87952210

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs876659456
dbSNP (classic)	rs876659456
ClinGen	rs876659456
ebi	rs876659456
HLI	rs876659456
Exac	rs876659456
Gnomad	rs876659456
Varsome	rs876659456
LitVar	rs876659456
Map	rs876659456
PheGenI	rs876659456
Biobank	rs876659456
1000 genomes	rs876659456
hgdp	rs876659456
ensembl	rs876659456
geneview	rs876659456
scholar	rs876659456
google	rs876659456
pharmgkb	rs876659456
gwascentral	rs876659456
openSNP	rs876659456
23andMe	rs876659456
SNPshot	rs876659456
SNPdbe	rs876659456
MSV3d	rs876659456
GWAS Ctlg	rs876659456

Max Magnitude

6.3

ClinVar
Risk	rs876659456(T;T)
Alt	rs876659456(T;T)
Reference	Rs876659456(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000010.10:g.89711967dupT
CLNSRC
CLNACC	RCV000214428.1, RCV000300517.1,