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rs1057519779

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519779(C;C)
Make rs1057519779(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position11157242
GeneMTOR
is asnp
is mentioned by
dbSNPrs1057519779
dbSNP (old)rs1057519779
ClinGenrs1057519779
ebirs1057519779
HLIrs1057519779
Exacrs1057519779
Gnomadrs1057519779
Varsomers1057519779
LitVarrs1057519779
Maprs1057519779
PheGenIrs1057519779
Biobankrs1057519779
1000 genomesrs1057519779
hgdprs1057519779
ensemblrs1057519779
gopubmedrs1057519779
geneviewrs1057519779
scholarrs1057519779
googlers1057519779
pharmgkbrs1057519779
gwascentralrs1057519779
openSNPrs1057519779
23andMers1057519779
23andMe allrs1057519779
SNPshotrs1057519779
SNPdbers1057519779
MSV3drs1057519779
GWAS Ctlgrs1057519779
Max Magnitude0
ClinVar
Risk rs1057519779(C;C)
Alt rs1057519779(C;C)
Reference Rs1057519779(T;T)
Significance Pathogenic
Disease Kidney Carcinoma FOCAL CORTICAL DYSPLASIA
Variation info
Gene MTOR
CLNDBN Kidney Carcinoma FOCAL CORTICAL DYSPLASIA, TYPE II, SOMATIC
Reversed 1
HGVS NC_000001.10:g.11217299A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000422999.1, RCV000477729.1,