Overview

IDAllelesLocationGenome BuildSource
rs2431697T/Cchr5: 16045297138dbsnp146
rs2431697T/C chr5: 159879978 37dbsnp146_grch37
1kg_5_159812556T/C chr5: 160452971 38ImmunoChip
1kg_5_159812556T/C chr5: 159879978 37ImmunoChip
1kg_5_159812556T/C chr5: 159812556 36ImmunoChip

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Historical Ids

Old Marker IDNew Marker IDCurrent Marker IDdbSNP Build
rs59665217rs2431697rs2431697130
rs17411055rs2431697rs2431697123

Criteria

rs2431697 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 rs2431697 as derived from dbSNP:

    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 rs2431697, 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.