{{Rsnum
|rsid=7749924
|Gene=LINC00243
|Chromosome=6
|position=30830214
|Orientation=plus
|GMAF=0.1345
|Gene_s=LINC00243
|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 | 76.1 | 23.0 | 0.9
| HCB | 65.0 | 30.7 | 4.4
| JPT | 75.2 | 22.1 | 2.7
| YRI | 82.3 | 16.3 | 1.4
| ASW | 86.0 | 12.3 | 1.8
| CHB | 65.0 | 30.7 | 4.4
| CHD | 59.6 | 36.7 | 3.7
| GIH | 54.5 | 42.6 | 3.0
| LWK | 79.1 | 20.0 | 0.9
| MEX | 70.7 | 29.3 | 0.0
| MKK | 72.4 | 25.0 | 2.6
| TSI | 78.4 | 19.6 | 2.0
| 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=8E-6
  |OR=.22
  |ORtxt=[0.12-0.32] unit increase
  |OA=1
}}

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