{{Rsnum
|rsid=7927894
|Chromosome=11
|position=76590272
|Orientation=plus
|GMAF=0.2819
|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 | 38.9 | 43.4 | 17.7
| HCB | 62.5 | 33.1 | 4.4
| JPT | 71.7 | 26.5 | 1.8
| YRI | 46.9 | 42.2 | 10.9
| ASW | 42.1 | 56.1 | 1.8
| CHB | 62.5 | 33.1 | 4.4
| CHD | 61.5 | 34.9 | 3.7
| GIH | 57.4 | 34.7 | 7.9
| LWK | 52.7 | 38.2 | 9.1
| MEX | 55.2 | 37.9 | 6.9
| MKK | 51.9 | 37.8 | 10.3
| TSI | 34.3 | 49.0 | 16.7
| HapMapRevision=28
}}
[http://blog.23andme.com/2009/04/08/snpwatch-genetic-variation-may-increase-risk-for-atopic-dermatitis/ 23andMe blog] associated rs7927894(T) with [[Crohn’s disease]] 1.16x and atopic dermatitis

{{PMID Auto GWAS
|PMID=19349984
|Trait=Atopic dermatitis
|Title=A common variant on chromosome 11q13 is associated with atopic dermatitis
|RiskAllele=A
|Pval=8E-10
}}
{{PMID Auto GWAS
|PMID=18587394
|Trait=Crohn's disease
|Title=Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease
|RiskAllele=T
|Pval=1.0000000000000001E-9
|OR=1.16
|ORtxt=[NR]
|OA=1
}}

{{PharmGKB
|RSID=rs7927894
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:19349984; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: A common variant on chromosome 11q13 is associated with Dermatitis, Atopic. (Initial Sample Size: 939 cases, 975 controls, 1,097 family members; Replication Sample Size: 2,637 cases, 3,957 controls); (Region: 11q13.5; Reported Gene(s): C11orf30; Risk Allele: rs7927894-A); (p-value= 0.0000000008).This variant is associated with Dermatitis, Atopic.
|Drugs=
|Drug Classes=
|Diseases=Dermatitis, Atopic
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA164739858
}}

{{PMID Auto
|PMID=20109745
|Title=Chromosome 11q13.5 variant associated with childhood eczema: An effect supplementary to filaggrin mutations
|OA=1
}}

{{PMID Auto
|PMID=20706116
|Title=Genome-wide approaches to the etiology of eczema
}}

{{omim
|id=613064
|rsnum=7927894
}}

{{PMID Auto
|PMID=21752155
|Title=Genetic susceptibility to inflammation and colonic transit in lower functional gastrointestinal disorders: preliminary analysis
|OA=1
}}

{{PMID Auto
|PMID=22197932
|Title=Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis
|OA=1
}}

{{PMID Auto
|PMID=19068216
|Title=Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship.
|OA=1
}}

{{PMID Auto
|PMID=21304977
|Title=An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians.
|OA=1
}}

{{PMID Auto
|PMID=21429916
|Title=The eczema risk variant on chromosome 11q13 (rs7927894) in the population-based ALSPAC cohort: a novel susceptibility factor for asthma and hay fever.
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs7927894
|overall_frequency_n=42
|overall_frequency_d=128
|overall_frequency=0.328125
|n_genomes=32
|n_genomes_annotated=0
|n_haplomes=37
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

{{PMID Auto
|PMID=23557745
|Title=Association of the chromosome 11q13.5 variant with atopic dermatitis in Austrian patients
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}