rs10916207 - SNAP47
Magnitude 2.2 · 1 study on file
Reported associations
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A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome - Unknown journal (n.d.) · Unknown authors · PubMed 35332129
ABSTRACT: Carpal tunnel syndrome (CTS) is the most common entrapment neuropathy and has a largely unknown underlying biology. In a genome-wide association study of CTS (48,843 cases and 1,190,837 controls), we found 53 sequence variants at 50 loci associated with the syndrome. The most significant association is with a missense variant (p.Glu366Lys) in SERPINA1 that protects against CTS (P = 2.9 × 10−24, OR = 0.76). Through various functional analyses, we conclude that at least 22 genes mediate CTS risk and highlight the role of 19 CTS variants in the biology of the extracellular matrix. We show that the genetic component to the risk is higher in bilateral/recurrent/persistent cases than nonrecurrent/nonpersistent cases. Anthropometric traits including height and BMI are gen
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Lifestyle context
Concrete actions anchored to the cited research. We do not prescribe, we describe.
Screening
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carpal tunnel syndrome risk assessment Moderate
SNAP47 rs10916207 G allele strongly associated with increased carpal tunnel syndrome risk
Baseline clinical evaluation for carpal tunnel syndrome; review occupational ergonomic factors