KIAA1671
HGNC:29345 · SaudiVarKB evidence summary derived from retained literature mentions.
1Gene mentions
1Publications
12Linked variants
2Associated phenotypes
Associated phenotypes
Co-mentioned in KIAA1671 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| autism spectrum disorder | HP:0000729 | 1 | 1 |
| neurodevelopmental disorder | HP:0012759 | 1 | 1 |
Linked variants
Variants normalized to KIAA1671| Variant | HGVS / rsID | Articles | Mentions |
|---|---|---|---|
| rs5752063 | rs5752063 | 1 | 1 |
| rs12627825 | rs12627825 | 1 | 1 |
| rs67049052 | rs67049052 | 1 | 1 |
| rs10237910 | rs10237910 | 1 | 1 |
| rs7965350 | rs7965350 | 1 | 1 |
| rs3812536 | rs3812536 | 1 | 1 |
| rs9693108 | rs9693108 | 1 | 1 |
| rs1802752 | rs1802752 | 1 | 1 |
| rs3924871 | rs3924871 | 1 | 1 |
| rs7818 | rs7818 | 1 | 1 |
| rs9383844 | rs9383844 | 1 | 1 |
| rs9767113 | rs9767113 | 1 | 1 |
Population context
Reported in the same publications| Country / region | Group | Cohort | Articles |
|---|
No structured population context is available.
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 SocietyPubMed ↗