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rs1060500126

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060500126(A;G)
Make rs1060500126(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position87933223
GenePTEN
is asnp
is mentioned by
dbSNPrs1060500126
dbSNP (old)rs1060500126
ClinGenrs1060500126
ebirs1060500126
HLIrs1060500126
Exacrs1060500126
Gnomadrs1060500126
Varsomers1060500126
Maprs1060500126
PheGenIrs1060500126
Biobankrs1060500126
1000 genomesrs1060500126
hgdprs1060500126
ensemblrs1060500126
gopubmedrs1060500126
geneviewrs1060500126
scholarrs1060500126
googlers1060500126
pharmgkbrs1060500126
gwascentralrs1060500126
openSNPrs1060500126
23andMers1060500126
23andMe allrs1060500126
SNPshotrs1060500126
SNPdbers1060500126
MSV3drs1060500126
GWAS Ctlgrs1060500126
Max Magnitude0
ClinVar
Risk rs1060500126(G;G)
Alt rs1060500126(G;G)
Reference Rs1060500126(A;A)
Significance Probable-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.89692980A>G
CLNSRC
CLNACC RCV000475421.1, RCV000491012.1,