Overview

IDAllelesLocationGenome BuildSource
rs4672495G/Tchr2: 6229410938dbsnp146
rs4672495G/T chr2: 62521244 37dbsnp146_grch37
imm_2_62374748A/C chr2: 62294109 38ImmunoChip
imm_2_62374748A/C chr2: 62521244 37ImmunoChip
imm_2_62374748A/C chr2: 62374748 36ImmunoChip

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Historical Ids

Old Marker IDNew Marker IDCurrent Marker IDdbSNP Build
rs56576398rs4672495rs4672495130
rs17300894rs4672495rs4672495123
rs58313246rs4672495rs4672495130

Criteria

rs4672495 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 rs4672495 as derived from dbSNP:

    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 rs4672495, 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.