{{Rsnum
|rsid=947474
|Gene=DKFZp667F0711
|Chromosome=10
|position=6390450
|Orientation=plus
|GMAF=0.1997
|Gene_s=FCGR2C
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=137
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 72.6 | 23.9 | 3.5
| HCB | 72.3 | 25.5 | 2.2
| JPT | 69.9 | 30.1 | 0.0
| YRI | 40.1 | 51.0 | 8.8
| ASW | 45.6 | 42.1 | 12.3
| CHB | 72.3 | 25.5 | 2.2
| CHD | 75.2 | 23.9 | 0.9
| GIH | 66.3 | 30.7 | 3.0
| LWK | 36.4 | 50.9 | 12.7
| MEX | 81.0 | 17.2 | 1.7
| MKK | 50.0 | 40.4 | 9.6
| TSI | 61.8 | 34.3 | 3.9
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=18978792
|Trait=Type 1 diabetes
|Title=Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci
|RiskAllele=G
|Pval=4.0000000000000002E-9
|OR=1.10
|ORtxt=[1.03-1.18]
|OA=1
}}

{{omim
|desc=DIABETES MELLITUS, INSULIN-DEPENDENT; IDDM
|id=222100
|rsnum=947474
}}

{{PharmGKB
|RSID=rs947474
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:18978792; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. (Initial Sample Size: 3,561 cases, 4,646 controls; Replication Sample Size: 6,225 cases, 6,946 controls, 3,064 trios); (Region: 10p15.1; Reported Gene: PRKCQ; Risk Allele: rs947474-G) This variant is associated with Type 1 diabetes.
|Drugs=
|Drug Classes=
|Diseases=Diabetes Mellitus, Type 1
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA164740869
}}

{{PMID Auto
|PMID=20736230
|Title=A ChIP-seq defined genome-wide map of vitamin D receptor binding: Associations with disease and evolution
|OA=1
}}

{{PharmGKB
|RSID=rs947474
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:18978792; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. (Initial Sample Size: 3,561 cases, 4,646 controls; Replication Sample Size: 6,225 cases, 6,946 controls, 3,064 trios); (Region: 10p15.1; Reported Gene(s): PRKCQ; Risk Allele: rs947474-G); (p-value= 0.000000004).This variant is associated with Type 1 diabetes.
|Drugs=
|Drug Classes=
|Diseases=Diabetes Mellitus; Diabetes Mellitus, Type 1
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA164740761
}}

{{PMID Auto
|PMID=19073967
|Title=Shared and distinct genetic variants in type 1 diabetes and celiac disease.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs947474
|overall_frequency_n=99
|overall_frequency_d=128
|overall_frequency=0.773438
|n_genomes=54
|n_genomes_annotated=0
|n_haplomes=85
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

{{PMID Auto GWAS
  |PMID=24390342
  |Trait=Rheumatoid arthritis
  |Title=Genetics of rheumatoid arthritis contributes to biology and drug discovery.
  |RiskAllele=A
  |Pval=3E-10
  |OR=1.12
  |ORtxt=[1.08-1.16]
  }}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}