rs138336847

Orientation

plus

Stabilized

plus

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

Make rs138336847(A;A)

Reference

GRCh38.p7 38.3/149

Chromosome

10

Position

87952264

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs138336847
dbSNP (classic)	rs138336847
ClinGen	rs138336847
ebi	rs138336847
HLI	rs138336847
Exac	rs138336847
Gnomad	rs138336847
Varsome	rs138336847
LitVar	rs138336847
Map	rs138336847
PheGenI	rs138336847
Biobank	rs138336847
1000 genomes	rs138336847
hgdp	rs138336847
ensembl	rs138336847
geneview	rs138336847
scholar	rs138336847
google	rs138336847
pharmgkb	rs138336847
gwascentral	rs138336847
openSNP	rs138336847
23andMe	rs138336847
SNPshot	rs138336847
SNPdbe	rs138336847
MSV3d	rs138336847
GWAS Ctlg	rs138336847

Max Magnitude

6.3

ClinVar
Risk	rs138336847(A;A)
Alt	rs138336847(A;A)
Reference	Rs138336847(G;G)
Significance	Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN
CLNDBN	not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89712021G>A
CLNSRC
CLNACC	RCV000285177.1, RCV000491116.1,