{{Rsnum
|rsid=600753
|Gene=DYX1C1
|Chromosome=15
|position=55466995
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|GMAF=0.4697
|Gene_s=DYX1C1,DYX1C1-CCPG1
|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 | 33.6 | 45.1 | 21.2
| HCB | 55.5 | 38.7 | 5.8
| JPT | 38.9 | 44.2 | 16.8
| YRI | 5.5 | 32.9 | 61.6
| ASW | 7.0 | 43.9 | 49.1
| CHB | 55.5 | 38.7 | 5.8
| CHD | 52.3 | 40.4 | 7.3
| GIH | 23.8 | 58.4 | 17.8
| LWK | 12.7 | 47.3 | 40.0
| MEX | 58.6 | 41.4 | 0.0
| MKK | 17.9 | 52.6 | 29.5
| TSI | 21.6 | 58.8 | 19.6
| HapMapRevision=28
}}{{Venter SNP
|rsid=600753
|allele=C
|frequency=0.608
|uid=1103645618108
|type=homozygous_SNP
|hugo=CCPG1
|ensembl gene=ENSG00000128845
|ensembl transcript=ENST00000321149
|sift=TOLERATED
|disease=A chromosomal aberration involving DYX1C1 may be a cause of [[dyslexia]] (MIM:127700). Translocation t(2;15)(q11;q21).
}}

{{PMID Auto
|PMID=18288507
|Title=Structural genomic variation in ischemic stroke.
|OA=1
}}

{{PMID Auto
|PMID=19240663
|Title=Further evidence for DYX1C1 as a susceptibility factor for dyslexia.
}}

{{GET Evidence
|gene=DYX1C1
|aa_change=Glu191Gly
|aa_change_short=E191G
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs600753
|overall_frequency_n=4803
|overall_frequency_d=10640
|overall_frequency=0.45141
|n_genomes=43
|n_genomes_annotated=0
|n_haplomes=56
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.249
|nblosum100=6
|autoscore=0
|webscore=N
}}

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