rs17036350 Rat Genome Database

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Variant: rs17036350 -  Homo sapiens

RGD ID: 151311619
RS ID: rs17036350
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MTOR  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh38 1 11,111,169
JBrowse: View Region in Genome Browser (JBrowse)
Model



Experimental Factor Annotations    Click to see Annotation Detail View
Object SymbolSpeciesTermQualifierEvidenceWithReferenceNotesSourceOriginal Reference(s)
rs17036350Humancorneal topography  IAGP 405850206 GWAS_CATALOGPMID:21665993
GWAS QTLs Related by Peak Marker
Data has come from the GWAS Catalog   
QTL GWAS Catalog Study Disease Trait Study Size Risk Allele Risk Allele Frequency P Value P Value MLOG Peak Marker Reported Odds Ratio or Beta-coefficient Ontology Accession PubMed
GWAS700425_H GCST001101 Corneal curvature 2,008 Chinese ancestry inidividuals, 2,281 Malay ancestry individuals T 0.20 4E-13 12.398 rs17036350 0.178 corneal topography (EFO:0004345)
 PMID:21665993

Variant Details
Variant Transcripts
Gene Symbol:MTOR
Accession:XM_011541166
Location:INTRON

Gene Symbol:MTOR
Accession:NM_001386500
Location:INTRON

Gene Symbol:MTOR
Accession:XM_017000900
Location:INTRON

Gene Symbol:MTOR
Accession:NM_004958
Location:INTRON

Gene Symbol:MTOR
Accession:XM_047416724
Location:INTRON

Gene Symbol:MTOR
Accession:XM_047416721
Location:INTRON

Gene Symbol:MTOR
Accession:NM_001386501
Location:INTRON

Gene Symbol:MTOR
Accession:XR_007058581
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
GWAS Catalog GCST001101 GWAS Catalog