{{Rsnum
|rsid=7224668
|Gene=SLC38A10
|Chromosome=17
|position=81261988
|Orientation=plus
|GMAF=0.4426
|Gene_s=SLC38A10
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 31.0 | 48.7 | 20.4
| HCB | 6.6 | 43.8 | 49.6
| JPT | 16.8 | 47.8 | 35.4
| YRI | 78.9 | 21.1 | 0.0
| ASW | 71.9 | 26.3 | 1.8
| CHB | 6.6 | 43.8 | 49.6
| CHD | 7.3 | 41.3 | 51.4
| GIH | 9.9 | 43.6 | 46.5
| LWK | 73.6 | 23.6 | 2.7
| MEX | 27.6 | 39.7 | 32.8
| MKK | 75.5 | 23.9 | 0.6
| TSI | 29.4 | 51.0 | 19.6
| 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=3E-8
  |OR=.17
  |ORtxt=[0.11-0.23] unit increase
  |OA=1
}}

{{on chip | Illumina Human 1M}}