rs786204899

Orientation

plus

Stabilized

plus

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

Make rs786204899(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

87933080

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs786204899
dbSNP (classic)	rs786204899
ClinGen	rs786204899
ebi	rs786204899
HLI	rs786204899
Exac	rs786204899
Gnomad	rs786204899
Varsome	rs786204899
LitVar	rs786204899
Map	rs786204899
PheGenI	rs786204899
Biobank	rs786204899
1000 genomes	rs786204899
hgdp	rs786204899
ensembl	rs786204899
geneview	rs786204899
scholar	rs786204899
google	rs786204899
pharmgkb	rs786204899
gwascentral	rs786204899
openSNP	rs786204899
23andMe	rs786204899
SNPshot	rs786204899
SNPdbe	rs786204899
MSV3d	rs786204899
GWAS Ctlg	rs786204899

Max Magnitude

6.3

ClinVar
Risk	rs786204899(-;-)
Alt	rs786204899(-;-)
Reference	Rs786204899(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89692837delT
CLNSRC
CLNACC	RCV000169840.1,