IDAllelesLocationGenome BuildSource
rs13098911C/Tchr3: 4619370938dbsnp146
rs13098911C/T chr3: 46235201 37dbsnp146_grch37
imm_3_46210205T/C chr3: 46193709 38ImmunoChip
imm_3_46210205T/C chr3: 46235201 37ImmunoChip
imm_3_46210205T/C chr3: 46210205 36ImmunoChip


Historical Ids

Old Marker IDNew Marker IDCurrent Marker IDdbSNP Build


rs13098911 meets the following criteria:

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

Functional Information

Gene function properties for rs13098911 as derived from dbSNP:


    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).



    Populations data from Ensembl 1000 Genome data release May 2013:

    Linkage Disequilibrium Statistics

    LD Search Options

    Linkage disequilibrium (LD) statistics are calculated for rs13098911, 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.