{{Rsnum
|rsid=2235302
|Gene=SELP
|Chromosome=1
|position=169611052
|Orientation=minus
|GMAF=0.3999
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=SELP
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 30.8 | 41.5 | 27.7
| HCB | 2.2 | 35.6 | 62.2
| JPT | 6.7 | 24.4 | 68.9
| YRI | 33.3 | 47.6 | 19.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 2.2 | 35.6 | 62.2
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20167578
|Trait=Soluble levels of adhesion molecules
|Title=Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels
|RiskAllele=T
|Pval=4E-16
|OR=7.30
|ORtxt=[5.54-9.06] % decrease
|OA=1
}}

{{PMID|18187665|OA=1
}} Identification of genetic polymorphisms associated with risk for pulmonary hypertension in sickle cell disease.

{{PMID|20401335|OA=1
}} Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.

{{on chip | 23andMe v1}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}