Overview

IDAllelesLocationGenome BuildSource
rs240993T/Cchr6: 11135251138dbsnp146
rs240993T/C chr6: 111673714 37dbsnp146_grch37
rs240993A/G chr6: 111352511 38ImmunoChip
rs240993A/G chr6: 111673714 37ImmunoChip
rs240993A/G chr6: 111780407 36ImmunoChip

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Historical Ids

Old Marker IDNew Marker IDCurrent Marker IDdbSNP Build
rs17511139rs240993rs240993126
rs61096863rs240993rs240993130

Criteria

rs240993 meets the following criteria:

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

Functional Information

Gene function properties for rs240993 as derived from dbSNP:
  • in intron
Gene(s) at location of variation:  REV3L 

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 rs240993, 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.