{{Rsnum
|rsid=2659005
|Gene=SLC38A10
|Chromosome=17
|position=81244914
|Orientation=minus
|GMAF=0.4252
|Gene_s=SLC38A10
|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 | 19.4 | 55.6 | 25.0
| HCB | 50.4 | 44.5 | 5.1
| JPT | 36.9 | 52.3 | 10.8
| YRI | 0.0 | 0.0 | 100.0
| ASW | 1.8 | 19.6 | 78.6
| CHB | 50.4 | 44.5 | 5.1
| CHD | 51.9 | 44.4 | 3.7
| GIH | 40.6 | 46.5 | 12.9
| LWK | 0.0 | 8.3 | 91.7
| MEX | 36.2 | 37.9 | 25.9
| MKK | 0.0 | 0.0 | 0.0
| TSI | 23.8 | 49.5 | 26.7
| 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=2E-6
  |OR=.15
  |ORtxt=[0.09-0.217] unit decrease
  |OA=1
}}

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