rs121913292

Orientation

plus

Stabilized

plus

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

Make rs121913292(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

10

Position

87933148

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs121913292
dbSNP (classic)	rs121913292
ClinGen	rs121913292
ebi	rs121913292
HLI	rs121913292
Exac	rs121913292
Gnomad	rs121913292
Varsome	rs121913292
LitVar	rs121913292
Map	rs121913292
PheGenI	rs121913292
Biobank	rs121913292
1000 genomes	rs121913292
hgdp	rs121913292
ensembl	rs121913292
geneview	rs121913292
scholar	rs121913292
google	rs121913292
pharmgkb	rs121913292
gwascentral	rs121913292
openSNP	rs121913292
23andMe	rs121913292
SNPshot	rs121913292
SNPdbe	rs121913292
MSV3d	rs121913292
GWAS Ctlg	rs121913292

Max Magnitude

6.3

ClinVar
Risk	rs121913292(-;-)
Alt	rs121913292(-;-)
Reference	Rs121913292(G;G)
Significance	Pathogenic
Disease	Cowden syndrome 1
Variation	info
Gene	PTEN
CLNDBN	Cowden syndrome 1
Reversed	0
HGVS	NC_000010.10:g.89692905delG
CLNSRC
CLNACC	RCV000172822.1,