{{Rsnum
|rsid=4150167
|Gene=TAF1C
|Chromosome=16
|position=84180078
|Orientation=plus
|GMAF=0.008724
|Gene_s=TAF1C
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 8.1 | 91.9
| HCB | 0.0 | 0.7 | 99.3
| JPT | 0.0 | 0.9 | 99.1
| YRI | 0.0 | 2.1 | 97.9
| ASW | 0.0 | 1.8 | 98.2
| CHB | 0.0 | 0.7 | 99.3
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 1.0 | 99.0
| LWK | 0.0 | 1.8 | 98.2
| MEX | 0.0 | 1.8 | 98.2
| MKK | 0.6 | 10.3 | 89.0
| TSI | 0.0 | 2.9 | 97.1
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=22843504
  |Trait=Autism
  |Title=Individual common variants exert weak effects on the risk for autism spectrum disorderspi.
  |RiskAllele=
  |Pval=3E-7
  |OR=1.96
  |ORtxt=[1.52-2.56]
  |OA=1
}}

{{PMID Auto
|PMID=16400609
|Title=Single-nucleotide polymorphisms in NAGNAG acceptors are highly predictive for variations of alternative splicing.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}