Traits - Astigmatism susceptibility

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Astigmatism susceptibility

Vision

Corneal astigmatism is a refractive error caused by an irregular curvature of the cornea, leading to blurred vision at multiple distances.

GWAS work has identified variants linked to corneal shape and astigmatism susceptibility.

This result reflects research-level variation in eye biology and is not an eye exam or a vision prescription.

Eye growth, age, and other refractive conditions also influence actual astigmatism.

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Report markers
39 SNP entries
Genes
0
Research
1 study
Your report

Genetic tendency

Lower astigmatism susceptibility 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
rs1623169TTT92.99%
rs830557CT52.90%
rs11238956TCC17.13%
rs1129038TT21.50%
rs12913832GG82.27%
rs1353386AC14.80%
rs11084579--A66.60%
rs62075722--G84.48%
rs142566675--A0.16%
rs149846728--A94.90%
rs1579050--G42.50%
rs16971637--C95.90%
rs196052--62.20%
rs2445565--47.00%
rs9517490--C30.00%
rs10223780--G51.76%
rs10279904--T98.70%
rs10993820--G79.10%
rs112947941--G93.10%
rs115822495--T0.34%
rs11639295--T37.86%
rs117023057--98.40%
rs11955682--T2.78%
rs12032649--G61.40%
rs12473604--77.50%
rs12551905--C98.50%
rs138016380--97.60%
rs2763272--T11.50%
rs35313216--92.80%
rs4864857--C78.40%
rs56274409--T94.40%
rs61935843--91.80%
rs62169220--G85.00%
rs6434068--C28.23%
rs6536686--19.20%
rs6741982--G96.10%
rs72629670--G37.72%
rs75380963--T2.34%
rs7931326--G93.50%

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.

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Coverage: 6/39 SNP entries detected (15%).

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

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