{{Rsnum
|rsid=6140226
|Chromosome=20
|position=7245836
|Orientation=plus
|GMAF=0.4238
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LOC101929265
|Gene_s=LOC101929265
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 31.9 | 50.4 | 17.7
| HCB | 13.1 | 48.9 | 38.0
| JPT | 20.4 | 46.0 | 33.6
| YRI | 85.0 | 14.3 | 0.7
| ASW | 70.2 | 28.1 | 1.8
| CHB | 13.1 | 48.9 | 38.0
| CHD | 15.6 | 43.1 | 41.3
| GIH | 10.9 | 50.5 | 38.6
| LWK | 68.2 | 28.2 | 3.6
| MEX | 43.1 | 41.4 | 15.5
| MKK | 59.0 | 38.5 | 2.6
| TSI | 28.4 | 49.0 | 22.5
| HapMapRevision=28
}}{{PMID Auto
|PMID=23160099
|Title=A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9
|OA=1
}}

{{PMID Auto
|PMID=17186469
|Title=Mutations in the gene encoding the Wnt-signaling component R-spondin 4 (RSPO4) cause autosomal recessive anonychia.
|OA=1
}}

{{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}}