NUP153, nucleoporin 153, 9972

N. diseases: 25; N. variants: 13
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1006066
rs1006066
Entrez Id: 9972
Gene Symbol: NUP153
NUP153
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: rs10949435
rs10949435
Entrez Id: 9972
Gene Symbol: NUP153
NUP153
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: rs10949436
rs10949436
Entrez Id: 9972
Gene Symbol: NUP153
NUP153
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: rs11753865
rs11753865
Entrez Id: 9972
Gene Symbol: NUP153
NUP153
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: rs12199222
rs12199222
Entrez Id: 9972
Gene Symbol: NUP153
NUP153
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: rs16879902
rs16879902
Entrez Id: 9972
Gene Symbol: NUP153
NUP153
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: rs2274136
rs2274136
Entrez Id: 9972
Gene Symbol: NUP153
NUP153
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: rs4716165
rs4716165
Entrez Id: 9972
Gene Symbol: NUP153
NUP153
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: rs4716167
rs4716167
Entrez Id: 9972
Gene Symbol: NUP153
NUP153
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: rs6906499
rs6906499
Entrez Id: 9972
Gene Symbol: NUP153
NUP153
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: rs9350055
rs9350055
Entrez Id: 9972
Gene Symbol: NUP153
NUP153
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: rs9383307
rs9383307
Entrez Id: 9972
Gene Symbol: NUP153
NUP153
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: rs9396787
rs9396787
Entrez Id: 9972
Gene Symbol: NUP153
NUP153
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: rs12199222
rs12199222
Entrez Id: 9972
Gene Symbol: NUP153
NUP153
CUI: C0489786
Disease:
Height 		T 0.700 GeneticVariation GWASDB Many sequence variants affecting diversity of adult human height. 18391951 2008
dbSNP: rs12199222
rs12199222
Entrez Id: 9972
Gene Symbol: NUP153
NUP153
CUI: C0005890
Disease:
Body Height 		T 0.700 GeneticVariation GWASCAT Many sequence variants affecting diversity of adult human height. 18391951 2008