Overview

IDAllelesLocationGenome BuildSource
rs2050568C/Tchr1: 15780045138dbsnp146
rs2050568C/T chr1: 157770241 37dbsnp146_grch37
rs2050568T/C chr1: 157800451 38ImmunoChip
rs2050568T/C chr1: 157770241 37ImmunoChip
rs2050568T/C chr1: 156036865 36ImmunoChip

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Historical Ids

Old Marker IDNew Marker IDCurrent Marker IDdbSNP Build
rs57911764rs2050568rs2050568130

Criteria

rs2050568 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 rs2050568 as derived from dbSNP:
  • in intron
Gene(s) at location of variation:  FCRL1 

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 rs2050568, 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.