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rs1085308056

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome10
Position87957850
GenePTEN
is asnp
is mentioned by
dbSNPrs1085308056
dbSNP (classic)rs1085308056
ClinGenrs1085308056
ebirs1085308056
HLIrs1085308056
Exacrs1085308056
Gnomadrs1085308056
Varsomers1085308056
LitVarrs1085308056
Maprs1085308056
PheGenIrs1085308056
Biobankrs1085308056
1000 genomesrs1085308056
hgdprs1085308056
ensemblrs1085308056
geneviewrs1085308056
scholarrs1085308056
googlers1085308056
pharmgkbrs1085308056
gwascentralrs1085308056
openSNPrs1085308056
23andMers1085308056
23andMe allrs1085308056
SNPshotrs1085308056
SNPdbers1085308056
MSV3drs1085308056
GWAS Ctlgrs1085308056
Max Magnitude0
ClinVar
Risk rs1085308056(G;G)
Alt rs1085308056(G;G)
Reference Rs1085308056(C;C)
Significance 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.89717607C>G
CLNSRC
CLNACC RCV000490589.1, RCV000491647.1,