{{Rsnum
|rsid=2207790
|Gene=NFIA
|Chromosome=1
|position=61432295
|Orientation=minus
|GMAF=0.3967
|Gene_s=NFIA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 23.0 | 53.1 | 23.9
| HCB | 38.7 | 41.6 | 19.7
| JPT | 30.1 | 47.8 | 22.1
| YRI | 63.9 | 34.0 | 2.0
| ASW | 54.4 | 36.8 | 8.8
| CHB | 38.7 | 41.6 | 19.7
| CHD | 33.9 | 48.6 | 17.4
| GIH | 20.8 | 46.5 | 32.7
| LWK | 60.9 | 34.5 | 4.5
| MEX | 36.2 | 48.3 | 15.5
| MKK | 42.3 | 50.0 | 7.7
| TSI | 24.5 | 58.8 | 16.7
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23463857
  |Trait=Electrocardiographic conduction measures
  |Title=Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.
  |RiskAllele=A
  |Pval=6E-18
  |OR=.60
  |ORtxt=[NR] msec decrease
  |OA=1
}}

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