Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs242016
rs242016
Entrez Id: 84766
Gene Symbol: CRACR2A
CRACR2A
CUI: C0031099
Disease:
Periodontitis 		A 0.700 GeneticVariation GWASCAT Four SNPs on the gene EFCAB4B resulted significantly associated to localized periodontitis (P < 5 × 10<sup>-8</sup> ), with the best hit on the rs242016 SNP (P = 1.5 × 10<sup>-8</sup> ). 30284742 2018
dbSNP: rs242016
rs242016
Entrez Id: 84766
Gene Symbol: CRACR2A
CRACR2A
CUI: C0600298
Disease:
Periodontosis 		A 0.700 GeneticVariation GWASCAT A genome-wide association study identifies an association between variants in EFCAB4B gene and periodontal disease in an Italian isolated population. 30284742 2018
dbSNP: rs10774167
rs10774167
Entrez Id: 84766
Gene Symbol: CRACR2A
CRACR2A
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: rs10774168
rs10774168
Entrez Id: 84766
Gene Symbol: CRACR2A
CRACR2A
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: rs10848914
rs10848914
Entrez Id: 84766
Gene Symbol: CRACR2A
CRACR2A
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: rs11616055
rs11616055
Entrez Id: 84766
Gene Symbol: CRACR2A
CRACR2A
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: rs12370980
rs12370980
Entrez Id: 84766
Gene Symbol: CRACR2A
CRACR2A
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: rs12424031
rs12424031
Entrez Id: 84766
Gene Symbol: CRACR2A
CRACR2A
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: rs16930743
rs16930743
Entrez Id: 84766
Gene Symbol: CRACR2A
CRACR2A
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: rs16930744
rs16930744
Entrez Id: 84766
Gene Symbol: CRACR2A
CRACR2A
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: rs16930752
rs16930752
Entrez Id: 84766
Gene Symbol: CRACR2A
CRACR2A
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: rs16930761
rs16930761
Entrez Id: 84766
Gene Symbol: CRACR2A
CRACR2A
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: rs1808285
rs1808285
Entrez Id: 84766
Gene Symbol: CRACR2A
CRACR2A
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: rs7134115
rs7134115
Entrez Id: 84766
Gene Symbol: CRACR2A
CRACR2A
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: rs717596
rs717596
Entrez Id: 84766
Gene Symbol: CRACR2A
CRACR2A
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: rs7307214
rs7307214
Entrez Id: 84766
Gene Symbol: CRACR2A
CRACR2A
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: rs7972545
rs7972545
Entrez Id: 84766
Gene Symbol: CRACR2A
CRACR2A
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: rs887304
rs887304
Entrez Id: 84766
Gene Symbol: CRACR2A
CRACR2A
CUI: C0023890
Disease:
Liver Cirrhosis 		A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. 20708005 2010
dbSNP: rs887304
rs887304
Entrez Id: 84766
Gene Symbol: CRACR2A
CRACR2A
CUI: C0400966
Disease:
Non-alcoholic Fatty Liver Disease 		A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. 20708005 2010
dbSNP: rs242016
rs242016
Entrez Id: 84766
Gene Symbol: CRACR2A
CRACR2A
CUI: C4023559
Disease:
Localized periodontitis 		0.010 GeneticVariation BEFREE Four SNPs on the gene EFCAB4B resulted significantly associated to localized periodontitis (P < 5 × 10<sup>-8</sup> ), with the best hit on the rs242016 SNP (P = 1.5 × 10<sup>-8</sup> ). 30284742 2018