Overview

IDAllelesLocationGenome BuildSource
rs7495132C/Tchr15: 9062966938dbsnp146
rs7495132C/T chr15: 91172901 37dbsnp146_grch37
rs7495132T/C chr15: 90629669 38ImmunoChip
rs7495132T/C chr15: 91172901 37ImmunoChip
rs7495132T/C chr15: 88973905 36ImmunoChip

Jbrowse

Historical Ids

Old Marker IDNew Marker IDCurrent Marker IDdbSNP Build
rs60392649rs7495132rs7495132130

Criteria

rs7495132 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 rs7495132 as derived from dbSNP:
  • in intron
Gene(s) at location of variation:  CRTC3  CRTC3-AS1 

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 rs7495132, 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.