Overview

IDAllelesLocationGenome BuildSource
rs8081176T/Cchr17: 8031018738dbsnp146
rs8081176T/C chr17: 78283987 37dbsnp146_grch37
rs8081176T/C chr17: 80310187 38ImmunoChip
rs8081176T/C chr17: 78283987 37ImmunoChip
rs8081176T/C chr17: 75898582 36ImmunoChip

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Historical Ids

Old Marker IDNew Marker IDCurrent Marker IDdbSNP Build
rs56613269rs8081176rs8081176130
rs57313163rs8081176rs8081176130

Criteria

No results found

Functional Information

Gene function properties for rs8081176 as derived from dbSNP:
  • in intron
Gene(s) at location of variation:  RNF213 

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 rs8081176, 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.