{{Rsnum
|rsid=11652075
|Gene=CARD14
|Chromosome=17
|position=80205094
|Orientation=plus
|GMAF=0.4229
|Gene_s=CARD14
|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 | 18.8 | 52.7 | 28.6
| HCB | 22.6 | 48.9 | 28.5
| JPT | 18.6 | 47.8 | 33.6
| YRI | 63.7 | 31.5 | 4.8
| ASW | 52.6 | 40.4 | 7.0
| CHB | 22.6 | 48.9 | 28.5
| CHD | 18.3 | 54.1 | 27.5
| GIH | 34.0 | 57.0 | 9.0
| LWK | 63.6 | 30.9 | 5.5
| MEX | 50.9 | 40.4 | 8.8
| MKK | 60.6 | 35.5 | 3.9
| TSI | 30.7 | 56.4 | 12.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=23905699
|Title=SNP rs11652075 in the CARD14 Gene as a Risk Factor for Psoriasis (PSORS2) in a Spanish Cohort
}}

{{PMID Auto
|PMID=22521419
|Title=Rare and common variants in CARD14, encoding an epidermal regulator of NF-kappaB, in psoriasis.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}