{{Rsnum
|rsid=7325564
|Gene=LINC00371
|Chromosome=13
|position=51150528
|Orientation=plus
|GMAF=0.3196
|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 | 49.6 | 40.7 | 9.7
| HCB | 72.3 | 25.5 | 2.2
| JPT | 77.9 | 17.7 | 4.4
| YRI | 15.0 | 44.9 | 40.1
| ASW | 8.8 | 56.1 | 35.1
| CHB | 72.3 | 25.5 | 2.2
| CHD | 72.5 | 24.8 | 2.8
| GIH | 49.5 | 40.6 | 9.9
| LWK | 26.4 | 42.7 | 30.9
| MEX | 41.4 | 48.3 | 10.3
| MKK | 36.5 | 50.6 | 12.8
| TSI | 51.0 | 36.3 | 12.7
| 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=5E-6
  |OR=.25
  |ORtxt=[0.14-0.35] 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}}