rs1060500110

Orientation

plus

Stabilized

plus

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

Make rs1060500110(-;-)

Make rs1060500110(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

87958020

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs1060500110
dbSNP (classic)	rs1060500110
ClinGen	rs1060500110
ebi	rs1060500110
HLI	rs1060500110
Exac	rs1060500110
Gnomad	rs1060500110
Varsome	rs1060500110
LitVar	rs1060500110
Map	rs1060500110
PheGenI	rs1060500110
Biobank	rs1060500110
1000 genomes	rs1060500110
hgdp	rs1060500110
ensembl	rs1060500110
geneview	rs1060500110
scholar	rs1060500110
google	rs1060500110
pharmgkb	rs1060500110
gwascentral	rs1060500110
openSNP	rs1060500110
23andMe	rs1060500110
SNPshot	rs1060500110
SNPdbe	rs1060500110
MSV3d	rs1060500110
GWAS Ctlg	rs1060500110

Max Magnitude

0

ClinVar
Risk	rs1060500110(-;-)
Alt	rs1060500110(-;-)
Reference	Rs1060500110(G;G)
Significance	Probable-Pathogenic
Disease	PTEN hamartoma tumor syndrome
Variation	info
Gene	PTEN
CLNDBN	PTEN hamartoma tumor syndrome
Reversed	0
HGVS	NC_000010.10:g.89717777delG
CLNSRC
CLNACC	RCV000461085.1,