IQCM, IQ motif containing M, 285423

N. diseases: 6; N. variants: 12
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10030601
rs10030601
Entrez Id: 285423
Gene Symbol: IQCM
IQCM
CUI: C0014544
Disease:
Epilepsy 		C 0.800 GeneticVariation GWASCAT Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32. 22949513 2012
dbSNP: rs10030601
rs10030601
Entrez Id: 285423
Gene Symbol: IQCM
IQCM
CUI: C0014544
Disease:
Epilepsy 		C 0.800 GeneticVariation GWASDB Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32. 22949513 2012
dbSNP: rs1032823
rs1032823
Entrez Id: 285423
Gene Symbol: IQCM
IQCM
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: rs1503713
rs1503713
Entrez Id: 285423
Gene Symbol: IQCM
IQCM
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: rs1553427
rs1553427
Entrez Id: 285423
Gene Symbol: IQCM
IQCM
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: rs17488863
rs17488863
Entrez Id: 285423
Gene Symbol: IQCM
IQCM
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: rs17624758
rs17624758
Entrez Id: 285423
Gene Symbol: IQCM
IQCM
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: rs17624758
rs17624758
Entrez Id: 285423
Gene Symbol: IQCM
IQCM
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: rs17686774
rs17686774
Entrez Id: 285423
Gene Symbol: IQCM
IQCM
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: rs1910462
rs1910462
Entrez Id: 285423
Gene Symbol: IQCM
IQCM
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: rs4835587
rs4835587
Entrez Id: 285423;105377479
Gene Symbol: IQCM;LOC105377479
IQCM;LOC105377479
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: rs17026425
rs17026425
Entrez Id: 285423
Gene Symbol: IQCM
IQCM
CUI: C0007113
Disease:
Rectal Carcinoma 		0.700 GeneticVariation GWASCAT A genome wide association study on Newfoundland colorectal cancer patients' survival outcomes. 25866641 2015
dbSNP: rs17026425
rs17026425
Entrez Id: 285423
Gene Symbol: IQCM
IQCM
CUI: C0034885
Disease:
Rectal Neoplasms 		0.700 GeneticVariation GWASCAT A genome wide association study on Newfoundland colorectal cancer patients' survival outcomes. 25866641 2015
dbSNP: rs10003632
rs10003632
Entrez Id: 285423
Gene Symbol: IQCM
IQCM
CUI: C0428886
Disease:
Mean blood pressure 		0.700 GeneticVariation GWASDB Pathway-based genome-wide association analysis of coronary heart disease identifies biologically important gene sets. 22510845 2012
dbSNP: rs4835580
rs4835580
Entrez Id: 285423
Gene Symbol: IQCM
IQCM
CUI: C0027404
Disease:
Narcolepsy 		0.700 GeneticVariation GWASDB Genome-wide association database developed in the Japanese Integrated Database Project. 19629137 2009
dbSNP: rs17026425
rs17026425
Entrez Id: 285423
Gene Symbol: IQCM
IQCM
CUI: C4722085
Disease:
Malignant neoplasm of colon and/or rectum 		0.010 GeneticVariation BEFREE We observed suggestive evidence (<i>P</i> < 0.05) for eight variants (rs17026425, rs17057166, rs6854845, rs1728400, rs17693104, rs202280, rs6797464, and rs823920) in all colorectal cancer and two variants (rs17026425 and rs6854845) in rectal cancer that were concordant with previous reports. 31488414 2019
dbSNP: rs17026425
rs17026425
Entrez Id: 285423
Gene Symbol: IQCM
IQCM
CUI: C0009402
Disease:
Colorectal Carcinoma 		0.010 GeneticVariation BEFREE We observed suggestive evidence (<i>P</i> < 0.05) for eight variants (rs17026425, rs17057166, rs6854845, rs1728400, rs17693104, rs202280, rs6797464, and rs823920) in all colorectal cancer and two variants (rs17026425 and rs6854845) in rectal cancer that were concordant with previous reports. 31488414 2019