rs587776666

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;ACAAT)	6.3	PTEN hamartoma tumor syndrome
(ACAAT;ACAAT)	0	common in clinvar

Make rs587776666(-;-)

Reference

GRCh38 38.1/142

Chromosome

10

Position

87933106

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs587776666
dbSNP (classic)	rs587776666
ClinGen	rs587776666
ebi	rs587776666
HLI	rs587776666
Exac	rs587776666
Gnomad	rs587776666
Varsome	rs587776666
LitVar	rs587776666
Map	rs587776666
PheGenI	rs587776666
Biobank	rs587776666
1000 genomes	rs587776666
hgdp	rs587776666
ensembl	rs587776666
geneview	rs587776666
scholar	rs587776666
google	rs587776666
pharmgkb	rs587776666
gwascentral	rs587776666
openSNP	rs587776666
23andMe	rs587776666
SNPshot	rs587776666
SNPdbe	rs587776666
MSV3d	rs587776666
GWAS Ctlg	rs587776666

Max Magnitude

6.3

ClinVar
Risk	rs587776666(-;-)
Alt	rs587776666(-;-)
Reference	Rs587776666(ACAAT;ACAAT)
Significance	Pathogenic
Disease	Cowden syndrome 1 PTEN hamartoma tumor syndrome
Variation	info
Gene	PTEN
CLNDBN	Cowden syndrome 1 PTEN hamartoma tumor syndrome
Reversed	0
HGVS	NC_000010.10:g.89692863_89692867delACAAT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008262.2, RCV000460680.1,