Traits - Bunions susceptibility

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Bunions susceptibility

Physical Traits

Hallux valgus (bunions) is a deformity of the joint at the base of the big toe, with strong heritable and biomechanical contributions.

GWAS work has identified variants linked to bunion susceptibility, often near genes involved in foot development.

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

Footwear, foot biomechanics, body weight, age, and prior injuries all strongly affect actual bunion development.

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

Genetic tendency

Average genetic tendency

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Explore the evidence

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
rs4811981TT30.00%
rs347133AA26.00%
rs11707593--T24.00%
rs2631419--T32.00%
rs71218579--68.00%
rs76655016--A1.00%
rs77993129--C97.00%
rs79147928--A86.00%
rs80177909--G98.00%
rs11868764--G3.00%
rs113871023--T99.00%
rs116783165--C3.00%
rs117155606--T1.00%
rs11728629--A24.00%
rs117974989--A99.00%
rs12143200--G3.00%
rs12888772--18.00%
rs140687271--A99.00%
rs146496015--T6.00%
rs58302722--A2.00%
rs12619631--A15.00%
rs539720802--T99.00%
rs13147821--26.00%
rs139705512--A2.00%
rs116712252--A99.00%
chr18:50130115--2.00%
chr8:52512282--1.00%
rs10176968--A39.00%
rs140676665--99.00%
rs141161671--A1.00%
rs142973841--T2.00%
rs145025296--C2.00%
rs1859504--C32.00%
rs188650377--T1.00%
rs191124187--C1.00%
rs28395286--T5.00%
rs3891969--A15.00%
rs55807512--C4.00%
rs6733149--C1.00%
rs72762109--G1.00%
rs74863661--T15.00%
rs78762426--A8.00%
rs9850315--C2.00%
rs150013648--T2.00%

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: 2/44 SNP entries detected (4%).

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

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