rs786204900

Orientation

plus

Stabilized

plus

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

Make rs786204900(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

87933250

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs786204900
dbSNP (classic)	rs786204900
ClinGen	rs786204900
ebi	rs786204900
HLI	rs786204900
Exac	rs786204900
Gnomad	rs786204900
Varsome	rs786204900
LitVar	rs786204900
Map	rs786204900
PheGenI	rs786204900
Biobank	rs786204900
1000 genomes	rs786204900
hgdp	rs786204900
ensembl	rs786204900
geneview	rs786204900
scholar	rs786204900
google	rs786204900
pharmgkb	rs786204900
gwascentral	rs786204900
openSNP	rs786204900
23andMe	rs786204900
SNPshot	rs786204900
SNPdbe	rs786204900
MSV3d	rs786204900
GWAS Ctlg	rs786204900

Max Magnitude

6.3

ClinVar
Risk	rs786204900(-;-)
Alt	rs786204900(-;-)
Reference	Rs786204900(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome PTEN hamartoma tumor syndrome
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome PTEN hamartoma tumor syndrome
Reversed	0
HGVS	NC_000010.10:g.89693007delA
CLNSRC
CLNACC	RCV000169841.1, RCV000477296.1,