{{Rsnum
|rsid=6436915
|Gene=SP110
|Chromosome=2
|position=230169808
|Orientation=plus
|GMAF=0.3669
|Gene_s=SP110
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 31.2 | 43.8 | 25.0
| HCB | 52.2 | 39.6 | 8.2
| JPT | 55.0 | 38.7 | 6.3
| YRI | 44.5 | 48.6 | 6.8
| ASW | 35.1 | 50.9 | 14.0
| CHB | 52.2 | 39.6 | 8.2
| CHD | 43.9 | 46.7 | 9.3
| GIH | 33.0 | 48.0 | 19.0
| LWK | 31.2 | 52.3 | 16.5
| MEX | 52.6 | 31.6 | 15.8
| MKK | 27.1 | 49.0 | 23.9
| TSI | 35.3 | 42.2 | 22.5
| HapMapRevision=28
}}{{PMID Auto
|PMID=21536091
|Title=Genetic association study suggests a role for SP110 variants in lymph node tuberculosis but not pulmonary tuberculosis in north Indians
}}

{{PMID|19456320|OA=1
}} A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.

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