{{Rsnum
|rsid=17147033
|Chromosome=7
|position=124366686
|Orientation=plus
|GMAF=0.1079
|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 | 94.7 | 5.3 | 0.0
| HCB | 62.0 | 33.6 | 4.4
| JPT | 56.6 | 37.2 | 6.2
| YRI | 93.2 | 6.8 | 0.0
| ASW | 87.7 | 12.3 | 0.0
| CHB | 62.0 | 33.6 | 4.4
| CHD | 54.6 | 42.6 | 2.8
| GIH | 79.2 | 20.8 | 0.0
| LWK | 85.5 | 14.5 | 0.0
| MEX | 75.9 | 24.1 | 0.0
| MKK | 76.9 | 21.8 | 1.3
| TSI | 97.1 | 2.9 | 0.0
| HapMapRevision=28
}}

{{omim
|desc=ALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME
|id=612079
|rsnum=17147033
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}