rs786204929

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;G)	6.3	Hereditary cancer predisposing syndrome
(G;G)	0	common in clinvar

Make rs786204929(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

87933144

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs786204929
dbSNP (classic)	rs786204929
ClinGen	rs786204929
ebi	rs786204929
HLI	rs786204929
Exac	rs786204929
Gnomad	rs786204929
Varsome	rs786204929
LitVar	rs786204929
Map	rs786204929
PheGenI	rs786204929
Biobank	rs786204929
1000 genomes	rs786204929
hgdp	rs786204929
ensembl	rs786204929
geneview	rs786204929
scholar	rs786204929
google	rs786204929
pharmgkb	rs786204929
gwascentral	rs786204929
openSNP	rs786204929
23andMe	rs786204929
SNPshot	rs786204929
SNPdbe	rs786204929
MSV3d	rs786204929
GWAS Ctlg	rs786204929

Max Magnitude

6.3

ClinVar
Risk	rs786204929(A;A)
Alt	rs786204929(A;A)
Reference	Rs786204929(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PTEN
CLNDBN	not provided
Reversed	0
HGVS	NC_000010.10:g.89692901G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000169874.3,