{{Rsnum
|rsid=4610302
|Chromosome=4
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SPARCL1
|position=87478958
|Gene_s=SPARCL1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 13.3 | 56.6 | 30.1
| HCB | 13.2 | 45.6 | 41.2
| JPT | 20.5 | 38.4 | 41.1
| YRI | 0.7 | 18.5 | 80.8
| ASW | 3.5 | 19.3 | 77.2
| CHB | 13.2 | 45.6 | 41.2
| CHD | 18.3 | 41.3 | 40.4
| GIH | 5.0 | 36.0 | 59.0
| LWK | 0.0 | 15.6 | 84.4
| MEX | 10.3 | 22.4 | 67.2
| MKK | 1.3 | 24.2 | 74.5
| TSI | 15.7 | 50.0 | 34.3
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=24121790
  |Trait=Esophageal adenocarcinoma
  |Title=A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus.
  |RiskAllele=G
  |Pval=4E-6
  |OR=1.18
  |ORtxt=[1.1-1.27]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}