Overview

IDAllelesLocationGenome BuildSource
rs72928038G/Achr6: 9026704938dbsnp146
rs72928038G/A chr6: 90976768 37dbsnp146_grch37
imm_6_91033489A/G chr6: 90267049 38ImmunoChip
imm_6_91033489A/G chr6: 90976768 37ImmunoChip
imm_6_91033489A/G chr6: 91033489 36ImmunoChip

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Historical Ids

Old Marker IDNew Marker IDCurrent Marker IDdbSNP Build

Criteria

rs72928038 meets the following criteria:

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

Functional Information

Gene function properties for rs72928038 as derived from dbSNP:
  • in intron
Gene(s) at location of variation:  BACH2 

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 rs72928038, 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.