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Peripheral arterial disease
These are the results of calculations comparing your genetic sequence to sequence of participants in studies published in the world literature on genetic risk for this disease.
How deCODEme calculates genetic riskConsult with our experts
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Relevant risk variants from the literature
Population: Males of European ancestry
| Locus | Chromo- some |
Variant / SNP | My Codes | Relative Risk |
Genotype frequency |
Num. Cases / Num. Controls |
|---|---|---|---|---|---|---|
| CHRNA3 / CHRNA5 / CHRNB4 | 15 | rs1051730 | CT | 1.05 | 44.9% | 2738 / 29964 |
| Thorgeirsson, TE et al. Nature. 2008 Apr 3;452(7187):638-42. | ||||||
View any SNP in the genome browser
Clicking on the SNP name will launch and/or sync the browser
Chromosome location of relevant variants
The figure below shows the genomic location of the relevant variants, represented as stripes across the chromosome. Their color indicates your relative risk (red: high risk, yellow: medium risk, green: low risk). Hover over the variants with the mouse cursor to obtain more detailed information.
Keep in mind
These are the results of calculations comparing your genetic sequence to sequence of participants in studies published in the world literature on genetic risk for this disease. Read more about how deCODEme calculates risks.
This test was developed and its performance characteristics determined by the deCODE genetics Diagnostic Laboratory. It has not been cleared or approved by the U. S. Food and Drug Administration (FDA).
