rs587776673

Orientation

plus

Stabilized

plus

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

Make rs587776673(-;-)

Reference

GRCh38 38.1/142

Chromosome

10

Position

87952132

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs587776673
dbSNP (classic)	rs587776673
ClinGen	rs587776673
ebi	rs587776673
HLI	rs587776673
Exac	rs587776673
Gnomad	rs587776673
Varsome	rs587776673
LitVar	rs587776673
Map	rs587776673
PheGenI	rs587776673
Biobank	rs587776673
1000 genomes	rs587776673
hgdp	rs587776673
ensembl	rs587776673
geneview	rs587776673
scholar	rs587776673
google	rs587776673
pharmgkb	rs587776673
gwascentral	rs587776673
openSNP	rs587776673
23andMe	rs587776673
SNPshot	rs587776673
SNPdbe	rs587776673
MSV3d	rs587776673
GWAS Ctlg	rs587776673

Max Magnitude

6.3

ClinVar
Risk	rs587776673(-;-)
Alt	rs587776673(-;-)
Reference	Rs587776673(C;C)
Significance	Pathogenic
Disease	Proteus-like syndrome PTEN hamartoma tumor syndrome
Variation	info
Gene	PTEN
CLNDBN	Proteus-like syndrome PTEN hamartoma tumor syndrome
Reversed	0
HGVS	NC_000010.10:g.89711889delC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008292.3, RCV000008293.3,