{{Rsnum
|rsid=2266928
|Gene=SOLH
|Chromosome=16
|position=530124
|Orientation=plus
|GMAF=0.3012
|Gene_s=SOLH
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 0.0 | 20.0 | 80.0
| HCB | 12.6 | 55.6 | 31.9
| JPT | 19.1 | 50.0 | 30.9
| YRI | 37.9 | 48.3 | 13.8
| ASW | 32.1 | 53.6 | 14.3
| CHB | 12.6 | 55.6 | 31.9
| CHD | 21.5 | 43.0 | 35.5
| GIH | 0.0 | 15.0 | 85.0
| LWK | 37.3 | 43.6 | 19.1
| MEX | 0.0 | 0.0 | 0.0
| MKK | 11.0 | 44.5 | 44.5
| TSI | 3.0 | 22.2 | 74.7
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23263863
  |Trait=Mean corpuscular hemoglobin concentration
  |Title=GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.
  |RiskAllele=A
  |Pval=3E-11
  |OR=.12
  |ORtxt=[0.083-0.152] unit decrease
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}