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rs1085308052

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome10
Position87952145
GenePTEN
is asnp
is mentioned by
dbSNPrs1085308052
dbSNP (old)rs1085308052
ClinGenrs1085308052
ebirs1085308052
HLIrs1085308052
Exacrs1085308052
Gnomadrs1085308052
Varsomers1085308052
Maprs1085308052
PheGenIrs1085308052
Biobankrs1085308052
1000 genomesrs1085308052
hgdprs1085308052
ensemblrs1085308052
gopubmedrs1085308052
geneviewrs1085308052
scholarrs1085308052
googlers1085308052
pharmgkbrs1085308052
gwascentralrs1085308052
openSNPrs1085308052
23andMers1085308052
23andMe allrs1085308052
SNPshotrs1085308052
SNPdbers1085308052
MSV3drs1085308052
GWAS Ctlgrs1085308052
Max Magnitude0
ClinVar
Risk rs1085308052(T;T)
Alt rs1085308052(T;T)
Reference Rs1085308052(-;-)
Significance Pathogenic
Disease PTEN hamartoma tumor syndrome
Variation info
Gene PTEN
CLNDBN PTEN hamartoma tumor syndrome
Reversed 0
HGVS NC_000010.10:g.89711902dup
CLNSRC
CLNACC RCV000490607.1,