rs786203477

Orientation

plus

Stabilized

plus

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

Make rs786203477(CT;CT)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

87894026

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs786203477
dbSNP (classic)	rs786203477
ClinGen	rs786203477
ebi	rs786203477
HLI	rs786203477
Exac	rs786203477
Gnomad	rs786203477
Varsome	rs786203477
LitVar	rs786203477
Map	rs786203477
PheGenI	rs786203477
Biobank	rs786203477
1000 genomes	rs786203477
hgdp	rs786203477
ensembl	rs786203477
geneview	rs786203477
scholar	rs786203477
google	rs786203477
pharmgkb	rs786203477
gwascentral	rs786203477
openSNP	rs786203477
23andMe	rs786203477
SNPshot	rs786203477
SNPdbe	rs786203477
MSV3d	rs786203477
GWAS Ctlg	rs786203477

Max Magnitude

6.3

ClinVar
Risk	rs786203477(TC;TC)
Alt	rs786203477(TC;TC)
Reference	Rs786203477(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89653783_89653784insCT
CLNSRC
CLNACC	RCV000166796.1,