rs786204857

Orientation

plus

Stabilized

plus

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

Make rs786204857(A;T)

Make rs786204857(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

87933060

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs786204857
dbSNP (classic)	rs786204857
ClinGen	rs786204857
ebi	rs786204857
HLI	rs786204857
Exac	rs786204857
Gnomad	rs786204857
Varsome	rs786204857
LitVar	rs786204857
Map	rs786204857
PheGenI	rs786204857
Biobank	rs786204857
1000 genomes	rs786204857
hgdp	rs786204857
ensembl	rs786204857
geneview	rs786204857
scholar	rs786204857
google	rs786204857
pharmgkb	rs786204857
gwascentral	rs786204857
openSNP	rs786204857
23andMe	rs786204857
SNPshot	rs786204857
SNPdbe	rs786204857
MSV3d	rs786204857
GWAS Ctlg	rs786204857

Max Magnitude

0

ClinVar
Risk	rs786204857(T;T)
Alt	rs786204857(T;T)
Reference	Rs786204857(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.89692817A>T
CLNSRC
CLNACC	RCV000169795.1,