{{Rsnum
|rsid=11118620
|Gene=LOC100129376
|Chromosome=1
|position=220855166
|Orientation=plus
|GMAF=0.3246
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=HLX-AS1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 9.2 | 47.7 | 43.1
| HCB | 13.3 | 60.0 | 26.7
| JPT | 20.5 | 38.6 | 40.9
| YRI | 7.9 | 36.5 | 55.6
| ASW | 0.0 | 0.0 | 0.0
| CHB | 13.3 | 60.0 | 26.7
| 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=20445134
|Trait=Heart failure
|Title=The Association of Genome-Wide Variation with the Risk of Incident Heart Failure in Adults of European and African Ancestry: A Prospective Meta-Analysis from the CHARGE Consortium
|RiskAllele=
|Pval=0.000007
|OR=1.15
|ORtxt=[0.98-1.35]
|OA=1
}}