{{Rsnum
|rsid=4899329
|Gene=SLC8A3
|Chromosome=14
|position=70153925
|Orientation=plus
|GMAF=0.2796
|Gene_s=SLC8A3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 34.5 | 45.1 | 20.4
| HCB | 88.3 | 11.7 | 0.0
| JPT | 91.2 | 8.8 | 0.0
| YRI | 65.3 | 33.3 | 1.4
| ASW | 52.6 | 42.1 | 5.3
| CHB | 88.3 | 11.7 | 0.0
| CHD | 93.6 | 6.4 | 0.0
| GIH | 73.3 | 24.8 | 2.0
| LWK | 55.0 | 37.6 | 7.3
| MEX | 25.9 | 46.6 | 27.6
| MKK | 68.6 | 29.5 | 1.9
| TSI | 39.2 | 50.0 | 10.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23382691
  |Trait=IgG glycosylation
  |Title=Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.
  |RiskAllele=C
  |Pval=5E-6
  |OR=.14
  |ORtxt=[0.081-0.203] unit increase
  |OA=1
}}

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