Overview

IDAllelesLocationGenome BuildSource
rs10036748C/Tchr5: 15107858538dbsnp146
rs10036748C/T chr5: 150458146 37dbsnp146_grch37
imm_5_150438339A/G chr5: 151078585 38ImmunoChip
imm_5_150438339A/G chr5: 150458146 37ImmunoChip
imm_5_150438339A/G chr5: 150438339 36ImmunoChip
rs10036748A/G chr5: 151078585 38ImmunoChip
rs10036748A/G chr5: 150458146 37ImmunoChip
rs10036748A/G chr5: 150438339 36ImmunoChip

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Historical Ids

Old Marker IDNew Marker IDCurrent Marker IDdbSNP Build
rs61219024rs10036748rs10036748130

Criteria

rs10036748 meets the following criteria:

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

Functional Information

Gene function properties for rs10036748 as derived from dbSNP:
  • in intron
Gene(s) at location of variation:  TNIP1 

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 rs10036748, 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.