rs786204863

Orientation

plus

Stabilized

plus

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

Make rs786204863(G;T)

Make rs786204863(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

87952119

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs786204863
dbSNP (classic)	rs786204863
ClinGen	rs786204863
ebi	rs786204863
HLI	rs786204863
Exac	rs786204863
Gnomad	rs786204863
Varsome	rs786204863
LitVar	rs786204863
Map	rs786204863
PheGenI	rs786204863
Biobank	rs786204863
1000 genomes	rs786204863
hgdp	rs786204863
ensembl	rs786204863
geneview	rs786204863
scholar	rs786204863
google	rs786204863
pharmgkb	rs786204863
gwascentral	rs786204863
openSNP	rs786204863
23andMe	rs786204863
SNPshot	rs786204863
SNPdbe	rs786204863
MSV3d	rs786204863
GWAS Ctlg	rs786204863

Max Magnitude

0

ClinVar
Risk	rs786204863(T;T)
Alt	rs786204863(T;T)
Reference	Rs786204863(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89711876G>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000169803.1,