Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1060500110

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060500110(-;-)
Make rs1060500110(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position87958020
GenePTEN
is asnp
is mentioned by
dbSNPrs1060500110
dbSNP (old)rs1060500110
ClinGenrs1060500110
ebirs1060500110
HLIrs1060500110
Exacrs1060500110
Gnomadrs1060500110
Varsomers1060500110
Maprs1060500110
PheGenIrs1060500110
Biobankrs1060500110
1000 genomesrs1060500110
hgdprs1060500110
ensemblrs1060500110
gopubmedrs1060500110
geneviewrs1060500110
scholarrs1060500110
googlers1060500110
pharmgkbrs1060500110
gwascentralrs1060500110
openSNPrs1060500110
23andMers1060500110
23andMe allrs1060500110
SNPshotrs1060500110
SNPdbers1060500110
MSV3drs1060500110
GWAS Ctlgrs1060500110
Max Magnitude0
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,