JDP2, Jun dimerization protein 2, 122953

N. diseases: 26; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs55818536
rs55818536
Entrez Id: 122953
Gene Symbol: JDP2
JDP2
CUI: C0007117
Disease:
Basal cell carcinoma
C 0.700 GeneticVariation GWASCAT Combined analysis of keratinocyte cancers identifies novel genome-wide loci. 31174203 2019
dbSNP: rs55818536
rs55818536
Entrez Id: 122953
Gene Symbol: JDP2
JDP2
CUI: C0751676
Disease:
Basal Cell Cancer
C 0.700 GeneticVariation GWASCAT Combined analysis of keratinocyte cancers identifies novel genome-wide loci. 31174203 2019
dbSNP: rs55818536
rs55818536
Entrez Id: 122953
Gene Symbol: JDP2
JDP2
CUI: C0206710
Disease:
Basal Cell Neoplasm
C 0.700 GeneticVariation GWASCAT Combined analysis of keratinocyte cancers identifies novel genome-wide loci. 31174203 2019
dbSNP: rs175643
rs175643
Entrez Id: 122953
Gene Symbol: JDP2
JDP2
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: rs76616
rs76616
Entrez Id: 122953
Gene Symbol: JDP2
JDP2
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: rs76616
rs76616
Entrez Id: 122953
Gene Symbol: JDP2
JDP2
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: rs8215
rs8215
Entrez Id: 122953
Gene Symbol: JDP2
JDP2
CUI: C0007766
Disease:
Intracranial Aneurysm
0.010 GeneticVariation BEFREE The allele distribution of three SNPs (two intronic: rs741846; P=0.0041 and rs175646; P=0.0014, and one in the untranslated region: rs8215; P=0.019) and their genotype distribution showed significant association in the Japanese IA patients. 20452405 2010