rs587776669

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;A)	6.3	Cowden syndrome
(A;A)	0	common in clinvar

Make rs587776669(-;-)

Reference

GRCh38 38.1/142

Chromosome

10

Position

87957914

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs587776669
dbSNP (classic)	rs587776669
ClinGen	rs587776669
ebi	rs587776669
HLI	rs587776669
Exac	rs587776669
Gnomad	rs587776669
Varsome	rs587776669
LitVar	rs587776669
Map	rs587776669
PheGenI	rs587776669
Biobank	rs587776669
1000 genomes	rs587776669
hgdp	rs587776669
ensembl	rs587776669
geneview	rs587776669
scholar	rs587776669
google	rs587776669
pharmgkb	rs587776669
gwascentral	rs587776669
openSNP	rs587776669
23andMe	rs587776669
SNPshot	rs587776669
SNPdbe	rs587776669
MSV3d	rs587776669
GWAS Ctlg	rs587776669

Max Magnitude

6.3

ClinVar
Risk	rs587776669(-;-)
Alt	rs587776669(-;-)
Reference	Rs587776669(A;A)
Significance	Pathogenic
Disease	Cowden syndrome 1
Variation	info
Gene	PTEN
CLNDBN	Cowden syndrome 1
Reversed	0
HGVS	NC_000010.10:g.89717671delA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008268.3,