rs1060500119

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;TG)	6.3	PTEN hamartoma tumor syndrome
(TG;TG)	0	common/normal

Make rs1060500119(-;-)

Chromosome

10

Position

87957968

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs1060500119
dbSNP (classic)	rs1060500119
ClinGen	rs1060500119
ebi	rs1060500119
HLI	rs1060500119
Exac	rs1060500119
Gnomad	rs1060500119
Varsome	rs1060500119
LitVar	rs1060500119
Map	rs1060500119
PheGenI	rs1060500119
Biobank	rs1060500119
1000 genomes	rs1060500119
hgdp	rs1060500119
ensembl	rs1060500119
geneview	rs1060500119
scholar	rs1060500119
google	rs1060500119
pharmgkb	rs1060500119
gwascentral	rs1060500119
openSNP	rs1060500119
23andMe	rs1060500119
SNPshot	rs1060500119
SNPdbe	rs1060500119
MSV3d	rs1060500119
GWAS Ctlg	rs1060500119

Max Magnitude

6.3

Molecularly equivalent to rs780264945

ClinVar
Risk	rs1060500119(-;-)
Alt	rs1060500119(-;-)
Reference	Rs1060500119(TG;TG)
Significance	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.89717725_89717726delTG
CLNSRC
CLNACC	RCV000468421.1, RCV000491414.1,