{{Rsnum
|rsid=6716901
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SLC25A12
|position=171816943
|Gene_s=SLC25A12
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 3.5 | 26.5 | 69.9
| HCB | 0.7 | 10.9 | 88.3
| JPT | 1.8 | 17.7 | 80.5
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 3.5 | 96.5
| CHB | 0.7 | 10.9 | 88.3
| CHD | 0.9 | 10.1 | 89.0
| GIH | 0.0 | 17.8 | 82.2
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 6.9 | 93.1
| MKK | 0.0 | 1.3 | 98.7
| TSI | 0.0 | 16.7 | 83.3
| HapMapRevision=28
}}In a study size of 117 Caucasians with [[Asperger syndrome]] and 426 controls "Single nucleotide polymorphism rs6716901 in SLC25A12 gene is associated with Asperger syndrome" {{PMID|24679184}} found association of this [[SNP]]'s minor allele (A) in [[SLC25A12]] gene with [[Asperger syndrome]]. Minor allele (A) was associated with OR 1.70 (0.98-3.02) P=0.008 after correcting for multiple testing. The study did not replicate previously reported associations with [[rs2056202]] and [[rs3765166]] which authors speculate could be due to differences in diagnosing AS and heterogenity of sample, though they admit to limitation of sample size and lack of replication sample.

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}