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rs1057519916

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519916(A;T)
Make rs1057519916(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position11109320
GeneMTOR
is asnp
is mentioned by
dbSNPrs1057519916
dbSNP (old)rs1057519916
ClinGenrs1057519916
ebirs1057519916
HLIrs1057519916
Exacrs1057519916
Gnomadrs1057519916
Varsomers1057519916
Maprs1057519916
PheGenIrs1057519916
Biobankrs1057519916
1000 genomesrs1057519916
hgdprs1057519916
ensemblrs1057519916
gopubmedrs1057519916
geneviewrs1057519916
scholarrs1057519916
googlers1057519916
pharmgkbrs1057519916
gwascentralrs1057519916
openSNPrs1057519916
23andMers1057519916
23andMe allrs1057519916
SNPshotrs1057519916
SNPdbers1057519916
MSV3drs1057519916
GWAS Ctlgrs1057519916
Max Magnitude0
ClinVar
Risk rs1057519916(T;T)
Alt rs1057519916(T;T)
Reference Rs1057519916(A;A)
Significance Probable-Pathogenic
Disease Malignant neoplasm of body of uterus Renal cell carcinoma Adenocarcinoma of stomach Neoplasm of breast
Variation info
Gene MTOR
CLNDBN Malignant neoplasm of body of uterus Renal cell carcinoma Adenocarcinoma of stomach Neoplasm of breast
Reversed 1
HGVS NC_000001.10:g.11169377T>A
CLNSRC
CLNACC RCV000420686.1, RCV000427238.1, RCV000429674.1, RCV000437898.1,