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rs1085308042

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome10
Position87894076
GenePTEN
is asnp
is mentioned by
dbSNPrs1085308042
dbSNP (old)rs1085308042
ClinGenrs1085308042
ebirs1085308042
HLIrs1085308042
Exacrs1085308042
Gnomadrs1085308042
Varsomers1085308042
Maprs1085308042
PheGenIrs1085308042
Biobankrs1085308042
1000 genomesrs1085308042
hgdprs1085308042
ensemblrs1085308042
gopubmedrs1085308042
geneviewrs1085308042
scholarrs1085308042
googlers1085308042
pharmgkbrs1085308042
gwascentralrs1085308042
openSNPrs1085308042
23andMers1085308042
23andMe allrs1085308042
SNPshotrs1085308042
SNPdbers1085308042
MSV3drs1085308042
GWAS Ctlgrs1085308042
Max Magnitude0
ClinVar
Risk rs1085308042(A;A)
Alt rs1085308042(A;A)
Reference Rs1085308042(G;G)
Significance Pathogenic
Disease PTEN hamartoma tumor syndrome
Variation info
Gene PTEN
CLNDBN PTEN hamartoma tumor syndrome
Reversed 0
HGVS NC_000010.10:g.89653833G>A
CLNSRC
CLNACC RCV000490575.1,