ATF2, activating transcription factor 2, 1386

N. diseases: 122; N. variants: 17
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1153672
rs1153672
Entrez Id: 1386
Gene Symbol: ATF2
ATF2
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: rs1153676
rs1153676
Entrez Id: 1386
Gene Symbol: ATF2
ATF2
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: rs1153681
rs1153681
Entrez Id: 1386
Gene Symbol: ATF2
ATF2
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: rs1153681
rs1153681
Entrez Id: 1386
Gene Symbol: ATF2
ATF2
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: rs1153684
rs1153684
Entrez Id: 1386
Gene Symbol: ATF2
ATF2
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: rs11888507
rs11888507
Entrez Id: 1386
Gene Symbol: ATF2
ATF2
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: rs11894840
rs11894840
Entrez Id: 1386
Gene Symbol: ATF2
ATF2
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: rs13383680
rs13383680
Entrez Id: 1386
Gene Symbol: ATF2
ATF2
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: rs13388308
rs13388308
Entrez Id: 1386
Gene Symbol: ATF2
ATF2
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: rs17270532
rs17270532
Entrez Id: 1386
Gene Symbol: ATF2
ATF2
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: rs2178329
rs2178329
Entrez Id: 1386
Gene Symbol: ATF2
ATF2
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: rs2541066
rs2541066
Entrez Id: 1386
Gene Symbol: ATF2
ATF2
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: rs3771928
rs3771928
Entrez Id: 1386
Gene Symbol: ATF2
ATF2
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: rs7566401
rs7566401
Entrez Id: 1386
Gene Symbol: ATF2
ATF2
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: rs7571171
rs7571171
Entrez Id: 1386
Gene Symbol: ATF2
ATF2
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: rs79402775
rs79402775
Entrez Id: 1386;100126350
Gene Symbol: ATF2;MIR933
ATF2;MIR933
CUI: C0699791
Disease:
Stomach Carcinoma 		0.010 GeneticVariation BEFREE miR-933(rs79402775) may contribute to decreased susceptibility to GC and this SNP could be developed as a biomarker for GC prognosis. 28534360 2019
dbSNP: rs79402775
rs79402775
Entrez Id: 1386;100126350
Gene Symbol: ATF2;MIR933
ATF2;MIR933
CUI: C0024623
Disease:
Malignant neoplasm of stomach 		0.010 GeneticVariation BEFREE miR-933(rs79402775) may contribute to decreased susceptibility to GC and this SNP could be developed as a biomarker for GC prognosis. 28534360 2019
dbSNP: rs79402775
rs79402775
Entrez Id: 1386;100126350
Gene Symbol: ATF2;MIR933
ATF2;MIR933
CUI: C0948008
Disease:
Ischemic stroke 		0.010 GeneticVariation BEFREE Our pilot study showed a weak association of rs79402775 in miRNA-933 (<i>p</i> = 0.044) and a relatively strong association of rs35196866 in miRNA-4669 (<i>p</i> = 0.016) with IS. 31781304 2019
dbSNP: rs3845744
rs3845744
Entrez Id: 1386
Gene Symbol: ATF2
ATF2
CUI: C0678222
Disease:
Breast Carcinoma 		0.010 GeneticVariation BEFREE We did not find an overall association of the two loci with breast cancer</span> prognosis, while the hazard ratios of the two loci (AG/GG vs. AA) were significantly higher among postmenopausal women than premenopausal women (P = 0.046, 0.016 for TSG101 rs2292179 and ATF2 rs3845744, respectively). 26729199 2016
dbSNP: rs3845744
rs3845744
Entrez Id: 1386
Gene Symbol: ATF2
ATF2
CUI: C0006142
Disease:
Malignant neoplasm of breast 		0.010 GeneticVariation BEFREE We did not find an overall association of the two loci with breast cancer</span> prognosis, while the hazard ratios of the two loci (AG/GG vs. AA) were significantly higher among postmenopausal women than premenopausal women (P = 0.046, 0.016 for TSG101 rs2292179 and ATF2 rs3845744, respectively). 26729199 2016
dbSNP: rs79402775
rs79402775
Entrez Id: 1386;100126350
Gene Symbol: ATF2;MIR933
ATF2;MIR933
CUI: C0238463
Disease:
Papillary thyroid carcinoma 		0.010 GeneticVariation BEFREE Three SNPs (rs67106263 in mir-3144, GA versus GG, OR = 1.35, 1.09-1.68; rs4919510 in mir-608, CC versus GG/GC, OR = 0.76, 0.60-0.97; and rs79402775 in mir-933, AA versus GG/GA, OR = 1.76, 1.00-3.12) were associated with PTC risk. 25381599 2015
dbSNP: rs79402775
rs79402775
Entrez Id: 1386;100126350
Gene Symbol: ATF2;MIR933
ATF2;MIR933
CUI: C0154038
Disease:
Benign neoplasm of thyroid gland 		0.010 GeneticVariation BEFREE In addition, three SNPs (rs10061133 in mir-449b, rs79402775 in mir-933 and rs4919510 in mir-608) showed at least borderline correlations with the risk of BN. 25381599 2015
dbSNP: rs1231071385
rs1231071385
Entrez Id: 1386
Gene Symbol: ATF2
ATF2
CUI: C0025202
Disease:
melanoma 		0.010 GeneticVariation BEFREE To directly assess ATF2's role in me</span>lanoma development, we crossed a mouse melanoma model (Nras(Q61K)::Ink4a⁻/⁻) with mice expressing a transcriptionally inactive form of ATF2 in melanocytes. 21203491 2010