| Geno
|
Mag
|
Summary
|
| (C;C)
|
2
|
common but increased risk of autism
|
| (T;T)
|
2
|
rare decreased risk of autism
|
| OMIM | 606053 |
| Desc | AUTISM, SUSCEPTIBILITY TO, 5; AUTS5 |
| Variant | |
| Related | also |
| OMIM | 603667 |
| Desc | SOLUTE CARRIER FAMILY 25 (MITOCHONDRIAL CARRIER, ARALAR), MEMBER 12; |
| Variant | |
| Related | also |
[PMID 19913066] Association study of the SLC25A12 gene and autism in Han Chinese in Taiwan
[PMID 21609426
] A quantitative association study of SLC25A12 and restricted repetitive behavior traits in autism spectrum disorders
[PMID 15056512] Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism.
[PMID 16263864] Confirmation of association between autism and the mitochondrial aspartate/glutamate carrier SLC25A12 gene on chromosome 2q31.
[PMID 17894412] Autism-related routines and rituals associated with a mitochondrial aspartate/glutamate carrier SLC25A12 polymorphism.
[PMID 18348195] An analysis of candidate autism loci on chromosome 2q24-q33: evidence for association to the STK39 gene.
[PMID 19360665] Mitochondrial aspartate/glutamate carrier SLC25A12 gene is associated with autism.
[PMID 25921325] Association between genetic variants in SLC25A12 and risk of autism spectrum disorders: An integrated meta-analysis
] A quantitative association study of SLC25A12 and restricted repetitive behavior traits in autism spectrum disorders
