Overview

IDAllelesLocationGenome BuildSource
rs7536201T/Cchr1: 2496659338dbsnp146
rs7536201T/C chr1: 25293084 37dbsnp146_grch37
imm_1_25165671T/C chr1: 24966593 38ImmunoChip
imm_1_25165671T/C chr1: 25293084 37ImmunoChip
imm_1_25165671T/C chr1: 25165671 36ImmunoChip

Jbrowse

Historical Ids

Old Marker IDNew Marker IDCurrent Marker IDdbSNP Build
rs59987122rs7536201rs7536201130

Criteria

rs7536201 meets the following criteria:

Criteria Name
Details
Disease Tags
Marker is in r2>0.8 with an index SNP 
Marker is an index SNP in a Region 
Marker is GW-Significant in a Study 

Functional Information

Gene function properties for rs7536201 as derived from dbSNP:
  • in 5prime gene region
Gene(s) at location of variation:  RUNX3 

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 rs7536201, 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.