rs1060500126

Orientation

plus

Stabilized

plus

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

Make rs1060500126(A;G)

Make rs1060500126(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

87933223

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs1060500126
dbSNP (classic)	rs1060500126
ClinGen	rs1060500126
ebi	rs1060500126
HLI	rs1060500126
Exac	rs1060500126
Gnomad	rs1060500126
Varsome	rs1060500126
LitVar	rs1060500126
Map	rs1060500126
PheGenI	rs1060500126
Biobank	rs1060500126
1000 genomes	rs1060500126
hgdp	rs1060500126
ensembl	rs1060500126
geneview	rs1060500126
scholar	rs1060500126
google	rs1060500126
pharmgkb	rs1060500126
gwascentral	rs1060500126
openSNP	rs1060500126
23andMe	rs1060500126
SNPshot	rs1060500126
SNPdbe	rs1060500126
MSV3d	rs1060500126
GWAS Ctlg	rs1060500126

Max Magnitude

0

ClinVar
Risk	rs1060500126(G;G)
Alt	rs1060500126(G;G)
Reference	Rs1060500126(A;A)
Significance	Probable-Pathogenic
Disease	PTEN hamartoma tumor syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	PTEN
CLNDBN	PTEN hamartoma tumor syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.89692980A>G
CLNSRC
CLNACC	RCV000475421.1, RCV000491012.1,