Overview

IDAllelesLocationGenome BuildSource
rs1788097C/Tchr18: 6987645238dbsnp146
rs1788097C/T chr18: 67543688 37dbsnp146_grch37
imm_18_65694668A/G chr18: 69876452 38ImmunoChip
imm_18_65694668A/G chr18: 67543688 37ImmunoChip
imm_18_65694668A/G chr18: 65694668 36ImmunoChip

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Historical Ids

Old Marker IDNew Marker IDCurrent Marker IDdbSNP Build
rs17207238rs1788097rs1788097123
rs60163227rs1788097rs1788097130

Criteria

rs1788097 meets the following criteria:

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

Functional Information

Gene function properties for rs1788097 as derived from dbSNP:
  • in intron
Gene(s) at location of variation:  CD226 

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 rs1788097, 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.