rs114018400 - NAV2: Stuttering association
Upload your raw genetic data once, we'll show you which variants you carry and what the research says.
Key takeaways
- This variant is linked to stuttering with a strong effect size.
- The risk allele T increases likelihood of stuttering.
- It was studied in about 74 thousand individuals.
Key takeaways This variant is linked to stuttering with a strong effect size. The risk allele T increases likelihood of stuttering. It was studied in about 74 thousand individuals.
What the research says This variant is associated with stuttering reported effect size 3.75 p=3e-6 PMID 40721530 risk allele T.
Reported associations Stuttering (risk allele T increases likelihood of stuttering reported effect size 3.75 p=3e-6 in about 74 thousand individuals) [PMID 40721530].
Evidence quality The GWAS includes about 74 thousand participants and reports a strong association with stuttering effect size 3.75 p=3e-6. No lifestyle considerations on file for this variant.
Frequently asked questions
What does the rs114018400 NAV2 variant do?
It is a genetic marker associated with stuttering and has been studied in large GWAS.
Is rs114018400 linked to stuttering?
Yes it is strongly associated with stuttering based on the GWAS data.
Can this variant affect other traits?
The evidence only shows a link to stuttering; no other traits are reported.