{{Rsnum
|rsid=1547251
|Chromosome=6
|position=82696390
|Orientation=plus
|GMAF=0.4881
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 22.1 | 46.0 | 31.9
| HCB | 5.8 | 38.0 | 56.2
| JPT | 1.8 | 32.7 | 65.5
| YRI | 98.4 | 1.6 | 0.0
| ASW | 80.7 | 15.8 | 3.5
| CHB | 5.8 | 38.0 | 56.2
| CHD | 4.6 | 32.4 | 63.0
| GIH | 27.7 | 33.7 | 38.6
| LWK | 90.0 | 10.0 | 0.0
| MEX | 22.4 | 43.1 | 34.5
| MKK | 59.6 | 30.8 | 9.6
| TSI | 21.6 | 46.1 | 32.4
| 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=1547251
}}

{{PMID|17160898|OA=1
}} 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.

{{PMID|17903300|OA=1
}} Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project.

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