{{Rsnum
|rsid=16982743
|Gene=SIGLEC12
|Chromosome=19
|position=51501649
|Orientation=plus
|GMAF=0.1873
|Gene_s=SIGLEC12
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 3.5 | 28.3 | 68.1
| HCB | 0.7 | 8.0 | 91.2
| JPT | 0.0 | 5.3 | 94.7
| YRI | 15.6 | 46.9 | 37.4
| ASW | 7.0 | 49.1 | 43.9
| CHB | 0.7 | 8.0 | 91.2
| CHD | 0.0 | 8.3 | 91.7
| GIH | 0.0 | 19.8 | 80.2
| LWK | 21.8 | 38.2 | 40.0
| MEX | 1.7 | 27.6 | 70.7
| MKK | 9.0 | 37.8 | 53.2
| TSI | 7.8 | 32.4 | 59.8
| HapMapRevision=28
}}{{PMID Auto
|PMID=23690342
|Title=Pharmacogenomic Association of Nonsynonymous SNPs in SIGLEC12, A1BG, and the Selectin Region and Cardiovascular Outcomes
}}

{{PMID Auto
|PMID=19200524
|Title=A genome-wide survey of the prevalence and evolutionary forces acting on human nonsense SNPs.
|OA=1
}}

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