rs786204871

Orientation

plus

Stabilized

plus

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

Make rs786204871(G;G)

Make rs786204871(G;T)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

87957934

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs786204871
dbSNP (classic)	rs786204871
ClinGen	rs786204871
ebi	rs786204871
HLI	rs786204871
Exac	rs786204871
Gnomad	rs786204871
Varsome	rs786204871
LitVar	rs786204871
Map	rs786204871
PheGenI	rs786204871
Biobank	rs786204871
1000 genomes	rs786204871
hgdp	rs786204871
ensembl	rs786204871
geneview	rs786204871
scholar	rs786204871
google	rs786204871
pharmgkb	rs786204871
gwascentral	rs786204871
openSNP	rs786204871
23andMe	rs786204871
SNPshot	rs786204871
SNPdbe	rs786204871
MSV3d	rs786204871
GWAS Ctlg	rs786204871

Max Magnitude

0

ClinVar
Risk	rs786204871(G;G)
Alt	rs786204871(G;G)
Reference	Rs786204871(T;T)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89717691T>G
CLNSRC
CLNACC	RCV000169811.1,