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rs1057519917

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519917(A;A)
Make rs1057519917(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position11124517
GeneMTOR
is asnp
is mentioned by
dbSNPrs1057519917
dbSNP (old)rs1057519917
ClinGenrs1057519917
ebirs1057519917
HLIrs1057519917
Exacrs1057519917
Gnomadrs1057519917
Varsomers1057519917
Maprs1057519917
PheGenIrs1057519917
Biobankrs1057519917
1000 genomesrs1057519917
hgdprs1057519917
ensemblrs1057519917
gopubmedrs1057519917
geneviewrs1057519917
scholarrs1057519917
googlers1057519917
pharmgkbrs1057519917
gwascentralrs1057519917
openSNPrs1057519917
23andMers1057519917
23andMe allrs1057519917
SNPshotrs1057519917
SNPdbers1057519917
MSV3drs1057519917
GWAS Ctlgrs1057519917
Max Magnitude0
ClinVar
Risk rs1057519917(A;A)
Alt rs1057519917(A;A)
Reference Rs1057519917(T;T)
Significance Probable-Pathogenic
Disease Colorectal Neoplasms Renal cell carcinoma Glioblastoma Malignant melanoma of skin Uterine cervical neoplasms Papillary renal cell carcinoma Malignant neoplasm of body of uterus
Variation info
Gene MTOR
CLNDBN Colorectal Neoplasms Renal cell carcinoma Glioblastoma Malignant melanoma of skin Uterine cervical neoplasms Papillary renal cell carcinoma, sporadic Malignant neoplasm of body of uterus
Reversed 1
HGVS NC_000001.10:g.11184574A>T
CLNSRC
CLNACC RCV000421026.1, RCV000421682.1, RCV000427631.1, RCV000431722.1, RCV000434180.1, RCV000442076.1, RCV000442198.1,