{{Rsnum
|rsid=229526
|Gene=C1QTNF6
|Chromosome=22
|position=37185382
|Orientation=minus
|GMAF=0.1804
|Gene_s=C1QTNF6
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 59.3 | 36.3 | 4.4
| HCB | 77.4 | 20.4 | 2.2
| JPT | 87.6 | 11.5 | 0.9
| YRI | 49.7 | 42.2 | 8.2
| ASW | 49.1 | 47.4 | 3.5
| CHB | 77.4 | 20.4 | 2.2
| CHD | 82.6 | 17.4 | 0.0
| GIH | 70.3 | 28.7 | 1.0
| LWK | 51.8 | 44.5 | 3.6
| MEX | 82.8 | 17.2 | 0.0
| MKK | 66.7 | 30.1 | 3.2
| TSI | 68.3 | 29.7 | 2.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22493691
|Trait=None
|Title=Novel associations for hypothyroidism include known autoimmune risk loci.
|RiskAllele=C
|Pval=0.000009
|OR=1.2160
|ORtxt=None
|OA=1
}}

{{GET Evidence
|gene=C1QTNF6
|aa_change=Pro42Arg
|aa_change_short=P42R
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs229526
|overall_frequency_n=2578
|overall_frequency_d=10758
|overall_frequency=0.239636
|n_genomes=21
|n_genomes_annotated=0
|n_haplomes=22
|n_articles=0
|n_articles_annotated=0
|nblosum100=5
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}