rs869312775

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs869312775(A;G)

Make rs869312775(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

10

Position

87933103

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs869312775
dbSNP (classic)	rs869312775
ClinGen	rs869312775
ebi	rs869312775
HLI	rs869312775
Exac	rs869312775
Gnomad	rs869312775
Varsome	rs869312775
LitVar	rs869312775
Map	rs869312775
PheGenI	rs869312775
Biobank	rs869312775
1000 genomes	rs869312775
hgdp	rs869312775
ensembl	rs869312775
geneview	rs869312775
scholar	rs869312775
google	rs869312775
pharmgkb	rs869312775
gwascentral	rs869312775
openSNP	rs869312775
23andMe	rs869312775
SNPshot	rs869312775
SNPdbe	rs869312775
MSV3d	rs869312775
GWAS Ctlg	rs869312775

Max Magnitude

0

ClinVar
Risk	rs869312775(G;G)
Alt	rs869312775(G;G)
Reference	Rs869312775(A;A)
Significance	Probable-Pathogenic
Disease	Cowden syndrome
Variation	info
Gene	PTEN
CLNDBN	Cowden syndrome
Reversed	0
HGVS	NC_000010.10:g.89692860A>G
CLNSRC
CLNACC	RCV000210160.1,