rs3924871
rs3924871 · SaudiVarKB evidence summary derived from retained literature mentions.
1Variant mentions
1Publications
6Associated gene records
2Associated phenotype records
Associated gene records
Co-mentioned in the same publicationsAssociated phenotype records
Co-mentioned in the same publications| Phenotype | Identifier / context | Articles | Mentions |
|---|---|---|---|
| autism spectrum disorder | HP:0000729 | 1 | 1 |
| neurodevelopmental disorder | HP:0012759 | 1 | 1 |
Associated population records
Co-mentioned in the same publicationsNo retained population associations.
Supporting publications
1 records- 2025Integrative approaches to m6A and m5C RNA modifications in autism spectrum disorder revealing potential causal variants.Mammalian genome : official journal of the International Mammalian Genome Society1 mentions