Overview

IDAllelesLocationGenome BuildSource
rs10488631T/Cchr7: 12895412938dbsnp146
rs10488631T/C chr7: 128594183 37dbsnp146_grch37
imm_7_128381419A/G chr7: 128954129 38ImmunoChip
imm_7_128381419A/G chr7: 128594183 37ImmunoChip
imm_7_128381419A/G chr7: 128381419 36ImmunoChip

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Historical Ids

Old Marker IDNew Marker IDCurrent Marker IDdbSNP Build
rs57552079rs10488631rs10488631130
rs17338574rs10488631rs10488631123

Criteria

rs10488631 meets the following criteria:

Criteria Name
Details
Disease Tags
Marker is in r2>0.8 with an index SNP 
Marker is an index SNP in a Region 
Marker is GW-Significant in a Study 

Functional Information

Gene function properties for rs10488631 as derived from dbSNP:
  • in 3prime gene region
Gene(s) at location of variation:  TNPO3 

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 rs10488631, 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.