rs587776672

Orientation

plus

Stabilized

plus

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

Make rs587776672(-;-)

Reference

GRCh38 38.1/142

Chromosome

10

Position

87960894

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs587776672
dbSNP (classic)	rs587776672
ClinGen	rs587776672
ebi	rs587776672
HLI	rs587776672
Exac	rs587776672
Gnomad	rs587776672
Varsome	rs587776672
LitVar	rs587776672
Map	rs587776672
PheGenI	rs587776672
Biobank	rs587776672
1000 genomes	rs587776672
hgdp	rs587776672
ensembl	rs587776672
geneview	rs587776672
scholar	rs587776672
google	rs587776672
pharmgkb	rs587776672
gwascentral	rs587776672
openSNP	rs587776672
23andMe	rs587776672
SNPshot	rs587776672
SNPdbe	rs587776672
MSV3d	rs587776672
GWAS Ctlg	rs587776672

Max Magnitude

6.3

ClinVar
Risk	rs587776672(-;-)
Alt	rs587776672(-;-)
Reference	Rs587776672(G;G)
Significance	Pathogenic
Disease	Cowden syndrome 1
Variation	info
Gene	PTEN
CLNDBN	Cowden syndrome 1
Reversed	0
HGVS	NC_000010.10:g.89720651delG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008287.3,