Overview

IDAllelesLocationGenome BuildSource
rs1021156T/Cchr8: 7866356938dbsnp146
rs1021156T/C chr8: 79575804 37dbsnp146_grch37
1kg_8_79738359T/C chr8: 78663569 38ImmunoChip
1kg_8_79738359T/C chr8: 79575804 37ImmunoChip
1kg_8_79738359T/C chr8: 79738359 36ImmunoChip

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Historical Ids

Old Marker IDNew Marker IDCurrent Marker IDdbSNP Build
rs386511050rs1021156rs1021156142
rs59634539rs1021156rs1021156130

Criteria

rs1021156 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 rs1021156 as derived from dbSNP:
  • in intron

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 rs1021156, 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.