Overview

IDAllelesLocationGenome BuildSource
rs17695092T/Gchr5: 17391085038dbsnp146
rs17695092T/G chr5: 173337853 37dbsnp146_grch37
1kg_5_173270459A/C chr5: 173910850 38ImmunoChip
1kg_5_173270459A/C chr5: 173337853 37ImmunoChip
1kg_5_173270459A/C chr5: 173270459 36ImmunoChip

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Historical Ids

Old Marker IDNew Marker IDCurrent Marker IDdbSNP Build
rs60005177rs17695092rs17695092130

Criteria

rs17695092 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 rs17695092 as derived from dbSNP:
  • in intron
Gene(s) at location of variation:  CPEB4 

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 rs17695092, 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.