{{Rsnum
|rsid=1053266
|Gene=CCDC6
|Chromosome=10
|position=61552692
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=A
|GMAF=0.4587
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 23.9 | 51.3 | 24.8
| HCB | 36.8 | 45.1 | 18.0
| JPT | 29.1 | 49.1 | 21.8
| YRI | 5.5 | 36.6 | 57.9
| ASW | 10.5 | 35.1 | 54.4
| CHB | 36.8 | 45.1 | 18.0
| CHD | 41.7 | 47.2 | 11.1
| GIH | 21.8 | 50.5 | 27.7
| LWK | 3.7 | 32.1 | 64.2
| MEX | 33.3 | 52.6 | 14.0
| MKK | 5.1 | 37.2 | 57.7
| TSI | 23.0 | 51.0 | 26.0
| HapMapRevision=28
}}{{Venter SNP
|rsid=1053266
|allele=T
|frequency=
|uid=1103649952977
|type=homozygous_SNP
|hugo=CCDC6
|ensembl gene=ENSG00000108091
|ensembl transcript=ENST00000263102
|sift=
|disease=A chromosomal aberration involving CCDC6 is a cause of thyroid papillary carcinoma (PACT) (MIM:188550). Inversion inv(10)(q11.2;q21) generates the RET/CCDC6 (PTC1) oncogene.
}}

{{PMID Auto
|PMID=16385451
|Title=A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.
|OA=1
}}

{{GET Evidence
|gene=CCDC6
|aa_change=Pro470Thr
|aa_change_short=P470T
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1053266
|overall_frequency_n=4528
|overall_frequency_d=10758
|overall_frequency=0.420896
|n_genomes=36
|n_genomes_annotated=0
|n_haplomes=48
|n_articles=0
|n_articles_annotated=0
|nblosum100=4
|autoscore=0
|webscore=N
}}

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