Overview

IDAllelesLocationGenome BuildSource
rs7069750G/C,Tchr10: 8900261938dbsnp146
rs7069750G/C,T chr10: 90762376 37dbsnp146_grch37
rs7069750T/G chr10: 89002619 38ImmunoChip
rs7069750T/G chr10: 90762376 37ImmunoChip
rs7069750T/G chr10: 90752356 36ImmunoChip

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Historical Ids

Old Marker IDNew Marker IDCurrent Marker IDdbSNP Build
rs117553410rs7069750rs7069750132
rs57728779rs7069750rs7069750130

Criteria

rs7069750 meets the following criteria:

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

Functional Information

Gene function properties for rs7069750 as derived from dbSNP:
  • in intron
Gene(s) at location of variation:  FAS 

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 rs7069750, 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.