rs10750486 - NTM: worry association
Upload your raw genetic data once, we'll show you which variants you carry and what the research says.
Key takeaways
- The rs10750486 variant is linked to feeling worry.
- Effect size is small, p=3e-8.
- Risk allele A is the common version.
Key takeaways
- The rs10750486 variant is linked to feeling worry.
- Effect size is small, p=3e-8.
- Risk allele A is the common version.
What the research says This variant rs10750486 is associated with feeling worry. The reported effect size is 5.55, p=3e-8, in about 372 thousand individuals, risk/effect allele A.PMID 29500382
Reported associations Feeling worry **This variant is associated with feeling worry, a reported effect size of 5.55, p=3e-8, in about 372 thousand individuals, risk/effect allele A.PMID 29500382
Evidence quality The association is based on a GWAS of 372 thousand individuals and has not been replicated elsewhere.PMID 29500382
No lifestyle considerations on file for this variant.
Frequently asked questions
What does the NTM gene do?
The NTM gene encodes a nucleotidyltransferase enzyme involved in RNA processing.
Is rs10750486 linked to anxiety?
Yes, the variant is associated with feeling worry which can be considered a mild form of anxiety.
Can this SNP affect stress levels?
The evidence shows a small association between the SNP and feeling worry but not strong enough to predict higher stress.