Overview

IDAllelesLocationGenome BuildSource
rs11719975G/Cchr3: 1874409338dbsnp146
rs11719975G/C chr3: 18785585 37dbsnp146_grch37
1kg_3_18760589C/G chr3: 18744093 38ImmunoChip
1kg_3_18760589C/G chr3: 18785585 37ImmunoChip
1kg_3_18760589C/G chr3: 18760589 36ImmunoChip

Jbrowse

Historical Ids

Old Marker IDNew Marker IDCurrent Marker IDdbSNP Build
rs59590168rs11719975rs11719975130

Criteria

rs11719975 meets the following criteria:

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

Functional Information

Gene function properties for rs11719975 as derived from dbSNP:
  • in 5prime gene region

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 rs11719975, 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.