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rs1085308046

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome10
Position87933160
GenePTEN
is asnp
is mentioned by
dbSNPrs1085308046
dbSNP (old)rs1085308046
ClinGenrs1085308046
ebirs1085308046
HLIrs1085308046
Exacrs1085308046
Gnomadrs1085308046
Varsomers1085308046
Maprs1085308046
PheGenIrs1085308046
Biobankrs1085308046
1000 genomesrs1085308046
hgdprs1085308046
ensemblrs1085308046
gopubmedrs1085308046
geneviewrs1085308046
scholarrs1085308046
googlers1085308046
pharmgkbrs1085308046
gwascentralrs1085308046
openSNPrs1085308046
23andMers1085308046
23andMe allrs1085308046
SNPshotrs1085308046
SNPdbers1085308046
MSV3drs1085308046
GWAS Ctlgrs1085308046
Max Magnitude0
ClinVar
Risk rs1085308046(C;C)
Alt rs1085308046(C;C)
Reference Rs1085308046(T;T)
Significance Pathogenic
Disease PTEN hamartoma tumor syndrome
Variation info
Gene PTEN
CLNDBN PTEN hamartoma tumor syndrome
Reversed 0
HGVS NC_000010.10:g.89692917T>C
CLNSRC
CLNACC RCV000490616.1,