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rs1060500119

From SNPedia

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


Make rs1060500119(-;-)
Chromosome10
Position87957968
GenePTEN
is asnp
is mentioned by
dbSNPrs1060500119
dbSNP (old)rs1060500119
ClinGenrs1060500119
ebirs1060500119
HLIrs1060500119
Exacrs1060500119
Gnomadrs1060500119
Varsomers1060500119
Maprs1060500119
PheGenIrs1060500119
Biobankrs1060500119
1000 genomesrs1060500119
hgdprs1060500119
ensemblrs1060500119
gopubmedrs1060500119
geneviewrs1060500119
scholarrs1060500119
googlers1060500119
pharmgkbrs1060500119
gwascentralrs1060500119
openSNPrs1060500119
23andMers1060500119
23andMe allrs1060500119
SNPshotrs1060500119
SNPdbers1060500119
MSV3drs1060500119
GWAS Ctlgrs1060500119
Max Magnitude6.3

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,