{{Rsnum
|rsid=1369766
|Gene=RPS26P43
|Chromosome=18
|position=51492510
|Orientation=minus
|GMAF=0.4426
|Gene_s=RPS26P43
|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 | 32.7 | 57.5 | 9.7
| HCB | 10.9 | 47.4 | 41.6
| JPT | 18.6 | 40.7 | 40.7
| YRI | 2.0 | 25.2 | 72.8
| ASW | 5.3 | 38.6 | 56.1
| CHB | 10.9 | 47.4 | 41.6
| CHD | 11.0 | 45.9 | 43.1
| GIH | 25.7 | 59.4 | 14.9
| LWK | 7.3 | 34.9 | 57.8
| MEX | 36.2 | 46.6 | 17.2
| MKK | 6.4 | 38.5 | 55.1
| TSI | 22.5 | 54.9 | 22.5
| HapMapRevision=28
}}

{{omim
|desc=DIARRHEA 2, WITH MICROVILLOUS ATROPHY; DIAR2
|id=251850
|rsnum=1369766
}}

{{PMID Auto
|PMID=17564975
|Title=Autosomal dominant nonsyndromic cleft lip and palate: significant evidence of linkage at 18q21.1.
|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 | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}