Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4640633
rs4640633
Entrez Id: 5602
Gene Symbol: MAPK10
MAPK10
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: rs6838659
rs6838659
Entrez Id: 5602
Gene Symbol: MAPK10
MAPK10
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: rs4488910
rs4488910
Entrez Id: 5602
Gene Symbol: MAPK10
MAPK10
CUI: C0035227
Disease:
Respiratory Function Tests 		0.700 GeneticVariation GWASDB Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction. 22837378 2012
dbSNP: rs369576054
rs369576054
Entrez Id: 5602;83478
Gene Symbol: MAPK10;ARHGAP24
MAPK10;ARHGAP24
CUI: C0027819
Disease:
Neuroblastoma 		0.020 GeneticVariation BEFREE Functional characterization of naturally occurring mutants (P405R and P425L) of p73alpha and p73beta found in neuroblastoma and lung cancer. 11429704 2001
dbSNP: rs369576054
rs369576054
Entrez Id: 5602;83478
Gene Symbol: MAPK10;ARHGAP24
MAPK10;ARHGAP24
CUI: C0027819
Disease:
Neuroblastoma 		0.020 GeneticVariation BEFREE Recently, we have found two mutations of p73 with amino acid substitution (P405R and P425L) in primary neuroblastomas. 10383137 1999
dbSNP: rs55805125
rs55805125
Entrez Id: 5602
Gene Symbol: MAPK10
MAPK10
CUI: C2363973
Disease:
Chronic thromboembolic pulmonary hypertension 		0.010 GeneticVariation BEFREE In addition, we identified two CTEPH associated SNPs (rs3739817 and rs55805125). 26820968 2016
dbSNP: rs1257715362
rs1257715362
Entrez Id: 5602;83478
Gene Symbol: MAPK10;ARHGAP24
MAPK10;ARHGAP24
CUI: C1332979
Disease:
Childhood Lymphoma 		0.010 GeneticVariation BEFREE PCR-SSCP and direct DNA sequencing of exons 2 to 14 of p73 revealed a missense mutation in one primary lymphoma: a G-to-A transition, with Glu291Lys change. 11461077 2001
dbSNP: rs1257715362
rs1257715362
Entrez Id: 5602;83478
Gene Symbol: MAPK10;ARHGAP24
MAPK10;ARHGAP24
CUI: C1332206
Disease:
Adult Lymphoma 		0.010 GeneticVariation BEFREE PCR-SSCP and direct DNA sequencing of exons 2 to 14 of p73 revealed a missense mutation in one primary lymphoma: a G-to-A transition, with Glu291Lys change. 11461077 2001
dbSNP: rs1257715362
rs1257715362
Entrez Id: 5602;83478
Gene Symbol: MAPK10;ARHGAP24
MAPK10;ARHGAP24
CUI: C0024299
Disease:
Lymphoma 		0.010 GeneticVariation BEFREE PCR-SSCP and direct DNA sequencing of exons 2 to 14 of p73 revealed a missense mutation in one primary lymphoma: a G-to-A transition, with Glu291Lys change. 11461077 2001
dbSNP: rs369576054
rs369576054
Entrez Id: 5602;83478
Gene Symbol: MAPK10;ARHGAP24
MAPK10;ARHGAP24
CUI: C0242379
Disease:
Malignant neoplasm of lung 		0.010 GeneticVariation BEFREE Functional characterization of naturally occurring mutants (P405R and P425L) of p73alpha and p73beta found in neuroblastoma and lung cancer. 11429704 2001
dbSNP: rs369576054
rs369576054
Entrez Id: 5602;83478
Gene Symbol: MAPK10;ARHGAP24
MAPK10;ARHGAP24
CUI: C4086165
Disease:
Childhood Neuroblastoma 		0.010 GeneticVariation BEFREE Functional characterization of naturally occurring mutants (P405R and P425L) of p73alpha and p73beta found in neuroblastoma and lung cancer. 11429704 2001
dbSNP: rs369576054
rs369576054
Entrez Id: 5602;83478
Gene Symbol: MAPK10;ARHGAP24
MAPK10;ARHGAP24
CUI: C0700095
Disease:
Central neuroblastoma 		0.010 GeneticVariation BEFREE Functional characterization of naturally occurring mutants (P405R and P425L) of p73alpha and p73beta found in neuroblastoma and lung cancer. 11429704 2001
dbSNP: rs369576054
rs369576054
Entrez Id: 5602;83478
Gene Symbol: MAPK10;ARHGAP24
MAPK10;ARHGAP24
CUI: C1306460
Disease:
Primary malignant neoplasm of lung 		0.010 GeneticVariation BEFREE Functional characterization of naturally occurring mutants (P405R and P425L) of p73alpha and p73beta found in neuroblastoma and lung cancer. 11429704 2001
dbSNP: rs369576054
rs369576054
Entrez Id: 5602;83478
Gene Symbol: MAPK10;ARHGAP24
MAPK10;ARHGAP24
CUI: C0684249
Disease:
Carcinoma of lung 		0.010 GeneticVariation BEFREE Functional characterization of naturally occurring mutants (P405R and P425L) of p73alpha and p73beta found in neuroblastoma and lung cancer. 11429704 2001