{{Rsnum
|rsid=8111071
|Gene=RSPH6A
|Chromosome=19
|position=45804148
|Orientation=plus
|GMAF=0.03168
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=RSPH6A
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 83.2 | 16.8 | 0.0
| HCB | 99.3 | 0.7 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 93.0 | 7.0 | 0.0
| CHB | 99.3 | 0.7 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 95.0 | 5.0 | 0.0
| LWK | 99.1 | 0.9 | 0.0
| MEX | 87.9 | 10.3 | 1.7
| MKK | 88.5 | 11.5 | 0.0
| TSI | 88.2 | 11.8 | 0.0
| HapMapRevision=28
}}[[rs8111071]] has been reported in a large study to be associated with [[Crohn's disease]].

The risk allele (oriented to the dbSNP entry) is (G); the odds ratio associated with heterozygotes is 1.47 (CI 1.25-1.73), and for homozygotes, 1.28 (CI 0.56-2.88). {{PMID|17554300|OA=1
}}

{{PMID Auto GWAS
|PMID=21658281
|Trait=None
|Title=GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.
|RiskAllele=
|Pval=0.000004
|OR=2.0100
|ORtxt=[1.50-2.70]
|OA=1
}}

{{PMID Auto
|PMID=20018022
|Title=Replication of recently identified associated single-nucleotide polymorphisms from six autoimmune diseases in Genetic Analysis Workshop 16 rheumatoid arthritis data.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}