{{Rsnum
|rsid=9574309
|Gene=LINC00331
|Chromosome=13
|position=78807966
|Orientation=plus
|GMAF=0.4389
|Gene_s=LINC00331
|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 | 15.0 | 53.1 | 31.9
| HCB | 22.6 | 46.0 | 31.4
| JPT | 9.7 | 44.2 | 46.0
| YRI | 21.1 | 52.4 | 26.5
| ASW | 26.3 | 49.1 | 24.6
| CHB | 22.6 | 46.0 | 31.4
| CHD | 22.9 | 46.8 | 30.3
| GIH | 17.0 | 49.0 | 34.0
| LWK | 28.2 | 42.7 | 29.1
| MEX | 24.1 | 53.4 | 22.4
| MKK | 43.6 | 41.0 | 15.4
| TSI | 18.6 | 46.1 | 35.3
| 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=.16
  |ORtxt=[0.093-0.226] unit increase
  |OA=1
}}

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