rs786204932

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs786204932(A;T)

Make rs786204932(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

87933150

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs786204932
dbSNP (classic)	rs786204932
ClinGen	rs786204932
ebi	rs786204932
HLI	rs786204932
Exac	rs786204932
Gnomad	rs786204932
Varsome	rs786204932
LitVar	rs786204932
Map	rs786204932
PheGenI	rs786204932
Biobank	rs786204932
1000 genomes	rs786204932
hgdp	rs786204932
ensembl	rs786204932
geneview	rs786204932
scholar	rs786204932
google	rs786204932
pharmgkb	rs786204932
gwascentral	rs786204932
openSNP	rs786204932
23andMe	rs786204932
SNPshot	rs786204932
SNPdbe	rs786204932
MSV3d	rs786204932
GWAS Ctlg	rs786204932

Max Magnitude

0

ClinVar
Risk	rs786204932(T;T)
Alt	rs786204932(T;T)
Reference	Rs786204932(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89692907A>T
CLNSRC
CLNACC	RCV000169877.1,