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rs1057519915

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519915(G;G)
Make rs1057519915(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position11109318
GeneMTOR
is asnp
is mentioned by
dbSNPrs1057519915
dbSNP (classic)rs1057519915
ClinGenrs1057519915
ebirs1057519915
HLIrs1057519915
Exacrs1057519915
Gnomadrs1057519915
Varsomers1057519915
LitVarrs1057519915
Maprs1057519915
PheGenIrs1057519915
Biobankrs1057519915
1000 genomesrs1057519915
hgdprs1057519915
ensemblrs1057519915
geneviewrs1057519915
scholarrs1057519915
googlers1057519915
pharmgkbrs1057519915
gwascentralrs1057519915
openSNPrs1057519915
23andMers1057519915
SNPshotrs1057519915
SNPdbers1057519915
MSV3drs1057519915
GWAS Ctlgrs1057519915
Max Magnitude0
ClinVar
Risk rs1057519915(G;G)
Alt rs1057519915(G;G)
Reference Rs1057519915(T;T)
Significance Probable-Pathogenic
Disease Neoplasm of breast Malignant neoplasm of body of uterus Adenocarcinoma of stomach Renal cell carcinoma
Variation info
Gene MTOR
CLNDBN Neoplasm of breast Malignant neoplasm of body of uterus Adenocarcinoma of stomach Renal cell carcinoma
Reversed 1
HGVS NC_000001.10:g.11169375A>C
CLNSRC
CLNACC RCV000424860.1, RCV000435587.1, RCV000444491.1, RCV000444639.1,