rs1060500124

Orientation

plus

Stabilized

plus

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

Make rs1060500124(-;-)

Make rs1060500124(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

87933253

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs1060500124
dbSNP (classic)	rs1060500124
ClinGen	rs1060500124
ebi	rs1060500124
HLI	rs1060500124
Exac	rs1060500124
Gnomad	rs1060500124
Varsome	rs1060500124
LitVar	rs1060500124
Map	rs1060500124
PheGenI	rs1060500124
Biobank	rs1060500124
1000 genomes	rs1060500124
hgdp	rs1060500124
ensembl	rs1060500124
geneview	rs1060500124
scholar	rs1060500124
google	rs1060500124
pharmgkb	rs1060500124
gwascentral	rs1060500124
openSNP	rs1060500124
23andMe	rs1060500124
SNPshot	rs1060500124
SNPdbe	rs1060500124
MSV3d	rs1060500124
GWAS Ctlg	rs1060500124

Max Magnitude

0

ClinVar
Risk	rs1060500124(-;-)
Alt	rs1060500124(-;-)
Reference	Rs1060500124(T;T)
Significance	Probable-Pathogenic
Disease	PTEN hamartoma tumor syndrome
Variation	info
Gene	PTEN
CLNDBN	PTEN hamartoma tumor syndrome
Reversed	0
HGVS	NC_000010.10:g.89693010delT
CLNSRC
CLNACC	RCV000461359.1,