Traits - Rosacea susceptibility

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Rosacea susceptibility

Aging & Appearance

Rosacea is a chronic skin condition that causes facial redness, flushing, and sometimes bumps or visible blood vessels.

GWAS work has identified variants near HLA, IL-13, and other immune-related genes linked to rosacea susceptibility and symptom severity.

This result reflects research-level variation in skin biology and is not a clinical diagnosis.

Triggers (sun, heat, alcohol, spicy food, stress) and skin care strongly affect actual rosacea symptoms.

Selected sample
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Report markers
98 SNP entries
Genes
0
Research
1 study
Your report

Genetic tendency

Average genetic tendency

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Behind this report

Review the genes, tested markers and supporting research.

SNPs tested

These are the unique genetic markers analyzed for this trait. Genotypes showing "--" were not identified in your DNA file. Report marker totals can include repeated study entries; this table shows each SNP once.

Genotypes and reported variant frequencies
SNPChromosomeGenotypeVariant alleleFrequency
rs13223215CC9.23%
rs719802CC50.66%
rs77779142CTT10.60%
rs788731GA44.19%
rs1129038TTT17.69%
rs6598858CTT38.86%
rs847CC24.70%
rs11768410--T47.30%
rs118006792--C0.08%
rs12243257--A6.37%
rs138330605--G0.12%
rs142431388--G0.04%
rs143178873--17.21%
rs144882124--G0.12%
rs147606948--C0.36%
rs147863159--T0.12%
rs180789526--99.98%
rs183739760--99.98%
rs34278912--A12.98%
rs7075455--G45.89%
rs7130337--G51.70%
rs73705028--C5.73%
rs74500669--A0.92%
rs77184728--A0.14%
rs78911933--A6.65%
rs80105877--94.03%
rs1805007--T1.86%
rs146167956--T0.20%
rs58048037--71.51%
rs55775132--A7.23%
rs56934772--C9.40%
rs57390839--98.42%
rs1144710--A0.00%
rs11617859--T0.88%
rs11628905--97.82%
rs117322572--T0.76%
rs11758316--G11.50%
rs118174802--T1.10%
rs12203592--T3.67%
rs12239076--G26.60%
rs1264350--95.73%
rs12912427--G19.09%
rs12972593--47.24%
rs1369639--90.69%
rs180826669--T0.12%
rs185236232--G0.12%
rs188276406--C0.20%
rs190788988--T0.14%
rs191291131--T0.02%
rs191805855--G0.16%
rs192531874--0.00%
rs193183075--T0.06%
rs200814246--0.00%
rs201820102--C0.00%
rs202220630--74.66%
rs2078387--30.95%
rs28415045--69.43%
rs28671668--61.20%
rs2894254--G1.96%
rs3130614--A2.60%
rs3130976--C19.59%
rs3131115--T32.69%
rs3132451--C13.60%
rs3132580--96.17%
rs3132649--93.71%
rs35724443--90.32%
rs41317102--90.62%
rs4143333--G3.95%
rs4714034--T57.55%
rs476080--T5.35%
rs5005856--G43.53%
rs519417--A3.25%
rs59614521--T18.53%
rs62035769--51.58%
rs628839--32.97%
rs75561433--A2.72%
rs75570604--C2.10%
rs75853901--G0.06%
rs77704860--A17.49%
rs77937677--A7.33%
rs78529895--G6.39%
rs803141--T32.31%
rs9272729--92.31%
rs9853827--T31.63%
rs140328462--A3.21%
rs112004685--A0.00%
rs10191743--T91.81%
rs142065142--0.00%
rs142438673--97.60%
rs145553345--C1.36%
rs149851565--88.76%
rs151305263--A0.06%
rs16882975--T0.82%
rs16891982--G27.50%
rs10859273--T21.43%
rs11097129--G19.13%
rs113042278--92.07%
rs146907294--A0.22%

DNA Genics reports genotypes based on the 'positive' strand of the human genome reference sequence (build 37/HG19). Other companies may use the opposite strand, so genotypes may need conversion for comparison.

Research studies

The following peer-reviewed scientific studies support the genetic associations analyzed in this report.

Browse traits

Coverage: 7/98 SNP entries detected (7%).

Reference: Human Genome Build 37 (HG19). Other testing companies may report using the opposite strand, requiring conversion for comparison.

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