{{Rsnum
|rsid=5910578
|Gene=SLC25A43
|Chromosome=X
|position=119433739
|Orientation=plus
|GMAF=0.266
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=SLC25A43
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 62.8 | 17.7 | 19.5
| HCB | 52.6 | 27.0 | 20.4
| JPT | 49.6 | 30.1 | 20.4
| YRI | 81.0 | 10.2 | 8.8
| ASW | 64.9 | 21.1 | 14.0
| CHB | 52.6 | 27.0 | 20.4
| CHD | 45.9 | 25.7 | 28.4
| GIH | 63.4 | 22.8 | 13.9
| LWK | 80.0 | 12.7 | 7.3
| MEX | 62.1 | 22.4 | 15.5
| MKK | 77.6 | 12.8 | 9.6
| TSI | 62.7 | 18.6 | 18.6
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21623375
|Trait=None
|Title=Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.
|RiskAllele=C
|Pval=1E-7
|OR=1.3400
|ORtxt=[NR]
}}

{{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}}