IDAllelesLocationGenome BuildSource
rs6897932C/Tchr5: 3587447338dbsnp146
rs6897932C/T chr5: 35874575 37dbsnp146_grch37
imm_5_35910332T/C chr5: 35874473 38ImmunoChip
imm_5_35910332T/C chr5: 35874575 37ImmunoChip
imm_5_35910332T/C chr5: 35910332 36ImmunoChip


Historical Ids

Old Marker IDNew Marker IDCurrent Marker IDdbSNP Build


rs6897932 meets the following criteria:

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

Functional Information

Gene function properties for rs6897932 as derived from dbSNP:
  • in intron
  • has reference
  • has non-synonymous missense
Gene(s) at location of variation:  IL7R 


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 rs6897932, 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.