{{Rsnum
|rsid=16863118
|Gene=CLRN1-AS1
|Chromosome=3
|position=150979421
|Orientation=plus
|GMAF=0.2282
|Gene_s=CLRN1-AS1
|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 | 72.3 | 26.8 | 0.9
| HCB | 46.7 | 40.1 | 13.1
| JPT | 40.2 | 45.5 | 14.3
| YRI | 63.3 | 34.0 | 2.7
| ASW | 61.4 | 33.3 | 5.3
| CHB | 46.7 | 40.1 | 13.1
| CHD | 29.4 | 49.5 | 21.1
| GIH | 72.3 | 24.8 | 3.0
| LWK | 61.8 | 32.7 | 5.5
| MEX | 67.2 | 29.3 | 3.4
| MKK | 60.3 | 34.6 | 5.1
| TSI | 66.7 | 28.4 | 4.9
| 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=.18
  |ORtxt=[0.1-0.26] 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}}