Overview

IDAllelesLocationGenome BuildSource
rs17035378T/Cchr2: 6837182338dbsnp146
rs17035378T/C chr2: 68598955 37dbsnp146_grch37
imm_2_68452459T/C chr2: 68371823 38ImmunoChip
imm_2_68452459T/C chr2: 68598955 37ImmunoChip
imm_2_68452459T/C chr2: 68452459 36ImmunoChip

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Historical Ids

Old Marker IDNew Marker IDCurrent Marker IDdbSNP Build
rs59017545rs17035378rs17035378130

Criteria

rs17035378 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 rs17035378 as derived from dbSNP:
  • in 5prime gene region
  • in intron
Gene(s) at location of variation:  PLEK 

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 rs17035378, 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.