RS12608932 Unknown gene
Upload your DNA to see your genotype for this variant.
What This Variant Does
"rs12608932 is a SNP located in an intron of the UNC13A gene which encodes UNC13A, a protein involved..."
GWAS Studies (11)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Frontotemporal dementia (MTAG) | C | β: 0.064 | 7E-26 | PubMed |
| Amyotrophic lateral sclerosis | C | OR: 0.12 | 3E-25 | PubMed |
| Amyotrophic lateral sclerosis | C | OR: 0.13 | 9E-25 | PubMed |
| Amyotrophic lateral sclerosis | — | OR: 1.25 | 3E-14 | PubMed |
| Amyotrophic lateral sclerosis (sporadic) | — | β: 0.022 | 3E-10 | PubMed |
| Amyotrophic lateral sclerosis | C | OR: 1.18 | 2E-8 | PubMed |
| Amyotrophic lateral sclerosis | — | OR: 1.1 | 2E-8 | PubMed |
| Amyotrophic lateral sclerosis | C | OR: 1.37 | 5E-8 | PubMed |
| Amyotrophic lateral sclerosis in C9orf72 mutation positive individuals | — | OR: 1.21 | 4E-7 | PubMed |
| Amyotrophic lateral sclerosis (sporadic) | — | — | 6E-6 | PubMed |
| Frontotemporal dementia | C | OR: 1.46 | 7E-6 | PubMed |