Overview

IDAllelesLocationGenome BuildSource
rs1059513T/Cchr12: 5709592638dbsnp146
rs1059513T/C chr12: 57489709 37dbsnp146_grch37

Jbrowse

Historical Ids

Old Marker IDNew Marker IDCurrent Marker IDdbSNP Build
rs386514503rs1059513rs1059513142
rs3200213rs1059513rs1059513106
rs56970011rs1059513rs1059513130
rs17546997rs1059513rs1059513123

Criteria

rs1059513 meets the following criteria:

Criteria Name
Details
Disease Tags
Marker is GW-Significant in a Study 
Marker is an index SNP in a Region 

Functional Information

Gene function properties for rs1059513 as derived from dbSNP:
  • in 3prime gene region
  • in 3prime utr
Gene(s) at location of variation:  NAB2  STAT6 

Study

Studies containing regions of association that span this marker are shown below. Please note that when making comparisons across studies, that they may vary in terms of size, genotyping platform, and exclusion criteria. If the 'Odds Ratio' is less than 1 then the region is protective (alleles are marked as blue) otherwise it is susceptible (alleles marked as red).

StudyPublicationDiseaseRegionMarkerAllelesP-valueORMAFGene(s)

Populations

Populations data from Ensembl 1000 Genome data release May 2013:

Linkage Disequilibrium Statistics

LD Search Options

Linkage disequilibrium (LD) statistics are calculated for rs1059513, using the 1000 genomes data release May 2013. Calculations are performed with the snpStats R library, covering 1Mb either side of the marker; and with the following filters applied: MAF > 0.01, call rate < 0.9, and chi-squared test for deviation from HWE > 25.