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rs1060500124

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060500124(-;-)
Make rs1060500124(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position87933253
GenePTEN
is asnp
is mentioned by
dbSNPrs1060500124
dbSNP (old)rs1060500124
ClinGenrs1060500124
ebirs1060500124
HLIrs1060500124
Exacrs1060500124
Gnomadrs1060500124
Varsomers1060500124
Maprs1060500124
PheGenIrs1060500124
Biobankrs1060500124
1000 genomesrs1060500124
hgdprs1060500124
ensemblrs1060500124
gopubmedrs1060500124
geneviewrs1060500124
scholarrs1060500124
googlers1060500124
pharmgkbrs1060500124
gwascentralrs1060500124
openSNPrs1060500124
23andMers1060500124
23andMe allrs1060500124
SNPshotrs1060500124
SNPdbers1060500124
MSV3drs1060500124
GWAS Ctlgrs1060500124
Max Magnitude0
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,