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rs1085307113

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome1
Position11114338
GeneMTOR
is asnp
is mentioned by
dbSNPrs1085307113
dbSNP (old)rs1085307113
ClinGenrs1085307113
ebirs1085307113
HLIrs1085307113
Exacrs1085307113
Gnomadrs1085307113
Varsomers1085307113
LitVarrs1085307113
Maprs1085307113
PheGenIrs1085307113
Biobankrs1085307113
1000 genomesrs1085307113
hgdprs1085307113
ensemblrs1085307113
gopubmedrs1085307113
geneviewrs1085307113
scholarrs1085307113
googlers1085307113
pharmgkbrs1085307113
gwascentralrs1085307113
openSNPrs1085307113
23andMers1085307113
23andMe allrs1085307113
SNPshotrs1085307113
SNPdbers1085307113
MSV3drs1085307113
GWAS Ctlgrs1085307113
Max Magnitude0
ClinVar
Risk rs1085307113(A;A)
Alt rs1085307113(A;A)
Reference Rs1085307113(T;T)
Significance Pathogenic
Disease FOCAL CORTICAL DYSPLASIA
Variation info
Gene MTOR
CLNDBN FOCAL CORTICAL DYSPLASIA, TYPE II, SOMATIC
Reversed 1
HGVS NC_000001.10:g.11174395A>G; NC_000001.10:g.11174395A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000477731.1, RCV000477677.1,