rs786204903

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;TCAA)	6.3	Hereditary cancer predisposing syndrome
(ATCA;ATCA)	0	common in clinvar
(TCAA;TCAA)	0	common/normal

Make rs786204903(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

87957976

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs786204903
dbSNP (classic)	rs786204903
ClinGen	rs786204903
ebi	rs786204903
HLI	rs786204903
Exac	rs786204903
Gnomad	rs786204903
Varsome	rs786204903
LitVar	rs786204903
Map	rs786204903
PheGenI	rs786204903
Biobank	rs786204903
1000 genomes	rs786204903
hgdp	rs786204903
ensembl	rs786204903
geneview	rs786204903
scholar	rs786204903
google	rs786204903
pharmgkb	rs786204903
gwascentral	rs786204903
openSNP	rs786204903
23andMe	rs786204903
SNPshot	rs786204903
SNPdbe	rs786204903
MSV3d	rs786204903
GWAS Ctlg	rs786204903

Max Magnitude

6.3

ClinVar
Risk	rs786204903(-;-)
Alt	rs786204903(-;-)
Reference	Rs786204903(ATCA;ATCA)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89717733_89717736delTCAA
CLNSRC
CLNACC	RCV000169844.1,