CDCA8, cell division cycle associated 8, 55143

N. diseases: 41; N. variants: 13
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10908369
rs10908369
Entrez Id: 55143
Gene Symbol: CDCA8
CDCA8
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs11264087
rs11264087
Entrez Id: 55143
Gene Symbol: CDCA8
CDCA8
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs12119598
rs12119598
Entrez Id: 55143
Gene Symbol: CDCA8
CDCA8
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs12139097
rs12139097
Entrez Id: 55143
Gene Symbol: CDCA8
CDCA8
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs3762352
rs3762352
Entrez Id: 54955;55143
Gene Symbol: C1orf109;CDCA8
C1orf109;CDCA8
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs3790623
rs3790623
Entrez Id: 55143
Gene Symbol: CDCA8
CDCA8
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs3790623
rs3790623
Entrez Id: 55143
Gene Symbol: CDCA8
CDCA8
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs497705
rs497705
Entrez Id: 55143
Gene Symbol: CDCA8
CDCA8
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs557897
rs557897
Entrez Id: 55143
Gene Symbol: CDCA8
CDCA8
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs589927
rs589927
Entrez Id: 55143
Gene Symbol: CDCA8
CDCA8
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs661460
rs661460
Entrez Id: 55143
Gene Symbol: CDCA8
CDCA8
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs768659
rs768659
Entrez Id: 55143
Gene Symbol: CDCA8
CDCA8
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs140856315
rs140856315
Entrez Id: 55143
Gene Symbol: CDCA8
CDCA8
CUI: C1563716
Disease:
Thyroid Dysgenesis 		0.010 GeneticVariation BEFREE We identified the novel missense mutations p.S148F, p.R114Q and p.L177W in the BOREALIN gene in TD-affected families. 28025328 2017
dbSNP: rs35565540
rs35565540
Entrez Id: 55143
Gene Symbol: CDCA8
CDCA8
CUI: C1563716
Disease:
Thyroid Dysgenesis 		0.010 GeneticVariation BEFREE We identified the novel missense mutations p.S148F, p.R114Q and p.L177W in the BOREALIN gene in TD-affected families. 28025328 2017