{{Rsnum
|rsid=10089
|Gene=SLC12A2
|Chromosome=5
|position=128186851
|Orientation=plus
|GMAF=0.2461
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=SLC12A2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 61.9 | 32.7 | 5.3
| HCB | 40.9 | 40.9 | 18.2
| JPT | 38.9 | 47.8 | 13.3
| YRI | 63.3 | 33.3 | 3.4
| ASW | 68.4 | 29.8 | 1.8
| CHB | 40.9 | 40.9 | 18.2
| CHD | 47.7 | 43.1 | 9.2
| GIH | 68.3 | 30.7 | 1.0
| LWK | 55.5 | 39.1 | 5.5
| MEX | 50.0 | 36.2 | 13.8
| MKK | 57.4 | 32.3 | 10.3
| TSI | 69.6 | 28.4 | 2.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21139019
|Trait=None
|Title=A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum
|RiskAllele=
|Pval=0.000002
|OR=2.5600
|ORtxt=[1.79-3.70]
|OA=1
}}

{{PMID Auto
|PMID=18520591
|Title=Sequence variants in host cell factor C1 are associated with Meniere's disease.
|OA=1
}}

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