rs876661060

Orientation

plus

Stabilized

plus

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

Make rs876661060(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

10

Position

87933111

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs876661060
dbSNP (classic)	rs876661060
ClinGen	rs876661060
ebi	rs876661060
HLI	rs876661060
Exac	rs876661060
Gnomad	rs876661060
Varsome	rs876661060
LitVar	rs876661060
Map	rs876661060
PheGenI	rs876661060
Biobank	rs876661060
1000 genomes	rs876661060
hgdp	rs876661060
ensembl	rs876661060
geneview	rs876661060
scholar	rs876661060
google	rs876661060
pharmgkb	rs876661060
gwascentral	rs876661060
openSNP	rs876661060
23andMe	rs876661060
SNPshot	rs876661060
SNPdbe	rs876661060
MSV3d	rs876661060
GWAS Ctlg	rs876661060

Max Magnitude

6.3

ClinVar
Risk	rs876661060(-;-)
Alt	rs876661060(-;-)
Reference	Rs876661060(CA;CA)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PTEN
CLNDBN	not provided
Reversed	0
HGVS	NC_000010.10:g.89692868_89692869delCA
CLNSRC
CLNACC	RCV000222845.1,