{{Rsnum
|rsid=2068330
|Gene=KCNH7
|Chromosome=2
|position=162380880
|Orientation=minus
|GMAF=0.4174
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=KCNH7
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 13.8 | 49.2 | 36.9
| HCB | 73.3 | 26.7 | 0.0
| JPT | 65.9 | 25.0 | 9.1
| YRI | 66.7 | 25.4 | 7.9
| ASW | 0.0 | 0.0 | 0.0
| CHB | 73.3 | 26.7 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID|19156166|OA=1
}} A study of 591 French Caucasian multiple sclerosis trio families found no association between [[rs1990760]] or [[rs2068330]] and the disease, which did not confirm one previously reported study.

{{PMID Auto
|PMID=18285833
|Title=IFIH1-GCA-KCNH7 locus: influence on multiple sclerosis risk.
}}

{{PMID Auto
|PMID=18927125
|Title=IFIH1 polymorphisms are significantly associated with type 1 diabetes and IFIH1 gene expression in peripheral blood mononuclear cells.
|OA=1
}}

{{PMID Auto
|PMID=19956101
|Title=Overview of the Rapid Response data.
|OA=1
}}

{{PMID Auto
|PMID=19956106
|Title=Analysis of 19 genes for association with type I diabetes in the Type I Diabetes Genetics Consortium families.
|OA=1
}}

{{PMID Auto
|PMID=19956109
|Title=The Type I Diabetes Genetics Consortium 'Rapid Response' family-based candidate gene study: strategy, genes selection, and main outcome.
|OA=1
}}

{{PMID Auto
|PMID=19961590
|Title=The rs1990760 polymorphism within the IFIH1 locus is not associated with Graves' disease, Hashimoto's thyroiditis and Addison's disease.
|OA=1
}}

{{PMID Auto
|PMID=20644636
|Title=Study of transcriptional effects in Cis at the IFIH1 locus.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}