Overview

IDAllelesLocationGenome BuildSource
rs2488389G/Achr1: 19766201138dbsnp146
rs2488389G/A chr1: 197631141 37dbsnp146_grch37
imm_1_195897764A/G chr1: 197662011 38ImmunoChip
imm_1_195897764A/G chr1: 197631141 37ImmunoChip
imm_1_195897764A/G chr1: 195897764 36ImmunoChip

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Historical Ids

Old Marker IDNew Marker IDCurrent Marker IDdbSNP Build
rs58646477rs2488389rs2488389130

Criteria

rs2488389 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 rs2488389 as derived from dbSNP:
  • in intron
Gene(s) at location of variation:  DENND1B 

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 rs2488389, 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.