{{Rsnum
|rsid=623155
|Chromosome=6
|position=78557764
|Orientation=plus
|GMAF=0.4665
|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 | 30.1 | 44.2 | 25.7
| HCB | 47.4 | 46.7 | 5.8
| JPT | 48.6 | 40.5 | 10.8
| YRI | 16.3 | 51.0 | 32.7
| ASW | 12.3 | 57.9 | 29.8
| CHB | 47.4 | 46.7 | 5.8
| CHD | 54.1 | 43.1 | 2.8
| GIH | 32.7 | 43.6 | 23.8
| LWK | 12.7 | 47.3 | 40.0
| MEX | 28.1 | 54.4 | 17.5
| MKK | 20.5 | 53.8 | 25.6
| TSI | 32.4 | 52.0 | 15.7
| HapMapRevision=28
}}
A study in Arab families found that an autosomal dominant condition known as split hand/foot malformation with long bone deficiency 2 (SHFLD2) maps between two SNPs, [[rs623155]] and [[rs1547251]]. (Variation at these two SNPs themselves does not appear to cause split hand.) [http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=610685 OMIM]

 {{omim
|desc=SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 2; SHFLD2
|id=610685
|rsnum=623155
}}

{{PMID Auto
|PMID=17160898
|Title=Genomewide linkage scan for split-hand/foot malformation with long-bone deficiency in a large Arab family identifies two novel susceptibility loci on chromosomes 1q42.2-q43 and 6q14.1.
|OA=1
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}