rs786202918

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	6.3	Hereditary cancer predisposing syndrome

Make rs786202918(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

87957951

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs786202918
dbSNP (classic)	rs786202918
ClinGen	rs786202918
ebi	rs786202918
HLI	rs786202918
Exac	rs786202918
Gnomad	rs786202918
Varsome	rs786202918
LitVar	rs786202918
Map	rs786202918
PheGenI	rs786202918
Biobank	rs786202918
1000 genomes	rs786202918
hgdp	rs786202918
ensembl	rs786202918
geneview	rs786202918
scholar	rs786202918
google	rs786202918
pharmgkb	rs786202918
gwascentral	rs786202918
openSNP	rs786202918
23andMe	rs786202918
SNPshot	rs786202918
SNPdbe	rs786202918
MSV3d	rs786202918
GWAS Ctlg	rs786202918

Max Magnitude

6.3

ClinVar
Risk	rs786202918(T;T)
Alt	rs786202918(T;T)
Reference	Rs786202918(C;C)
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.89717708C>T
CLNSRC
CLNACC	RCV000165985.1, RCV000490581.1,