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rs1057524044

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057524044(C;C)
Make rs1057524044(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position11114326
GeneMTOR
is asnp
is mentioned by
dbSNPrs1057524044
dbSNP (classic)rs1057524044
ClinGenrs1057524044
ebirs1057524044
HLIrs1057524044
Exacrs1057524044
Gnomadrs1057524044
Varsomers1057524044
LitVarrs1057524044
Maprs1057524044
PheGenIrs1057524044
Biobankrs1057524044
1000 genomesrs1057524044
hgdprs1057524044
ensemblrs1057524044
geneviewrs1057524044
scholarrs1057524044
googlers1057524044
pharmgkbrs1057524044
gwascentralrs1057524044
openSNPrs1057524044
23andMers1057524044
SNPshotrs1057524044
SNPdbers1057524044
MSV3drs1057524044
GWAS Ctlgrs1057524044
Max Magnitude0
ClinVar
Risk rs1057524044(C;C)
Alt rs1057524044(C;C)
Reference Rs1057524044(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MTOR
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.11174383A>G
CLNSRC
CLNACC RCV000427422.1,