Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs8042861
rs8042861
Entrez Id: 8826
Gene Symbol: IQGAP1
IQGAP1
CUI: C0026769
Disease:
Multiple Sclerosis
0.710 GeneticVariation BEFREE Consistent allelic imbalance was observed for rs907091 in IKZF3 and rs11609 in IQGAP1, which are in strong linkage disequilibrium with the multiple sclerosis associated single nucleotide polymorphisms rs12946510 and rs8042861, respectively. 27080863 2016
dbSNP: rs8042861
rs8042861
Entrez Id: 8826
Gene Symbol: IQGAP1
IQGAP1
CUI: C0026769
Disease:
Multiple Sclerosis
A 0.710 GeneticVariation GWASCAT Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. 24076602 2013
dbSNP: rs11609
rs11609
Entrez Id: 8826
Gene Symbol: IQGAP1
IQGAP1
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2074585
rs2074585
Entrez Id: 8826
Gene Symbol: IQGAP1
IQGAP1
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2074585
rs2074585
Entrez Id: 8826
Gene Symbol: IQGAP1
IQGAP1
CUI: C0013595
Disease:
Eczema
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2074585
rs2074585
Entrez Id: 8826
Gene Symbol: IQGAP1
IQGAP1
CUI: C0427460
Disease:
Red cell distribution width determination
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2074585
rs2074585
Entrez Id: 8826
Gene Symbol: IQGAP1
IQGAP1
CUI: C0002170
Disease:
Alopecia
A 0.700 GeneticVariation GWASCAT Genetic prediction of male pattern baldness. 28196072 2017
dbSNP: rs3540
rs3540
Entrez Id: 8826
Gene Symbol: IQGAP1
IQGAP1
CUI: C1527304
Disease:
Allergic Reaction
G 0.700 GeneticVariation GWASCAT Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology. 29083406 2017
dbSNP: rs2074585
rs2074585
Entrez Id: 8826
Gene Symbol: IQGAP1
IQGAP1
CUI: C0200641
Disease:
Blood basophil count (lab test)
A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs3540
rs3540
Entrez Id: 8826
Gene Symbol: IQGAP1
IQGAP1
CUI: C0200635
Disease:
Lymphocyte Count measurement
A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs11609
rs11609
Entrez Id: 8826
Gene Symbol: IQGAP1
IQGAP1
CUI: C0026769
Disease:
Multiple Sclerosis
0.010 GeneticVariation BEFREE Using multiple sclerosis patients and healthy controls heterozygous for rs907091 and rs11609, we showed that the multiple sclerosis risk alleles at IKZF3 and IQGAP1 are expressed at higher levels as compared to the protective allele. 27080863 2016
dbSNP: rs1410483989
rs1410483989
Entrez Id: 8826
Gene Symbol: IQGAP1
IQGAP1
CUI: C0151718
Disease:
Hypocholesterolemia
0.010 GeneticVariation BEFREE Finally, genotype-phenotype correlation is not obvious in our cohort with CRD; even if, the Canadian subjects with the allele 409G>A had a more severe degree (P<0.001) of hypocholesterolemia than the other patients, many clinical data are inconsistent with a hypothetical genotype-phenotype correlation. 19285442 2009
dbSNP: rs1410483989
rs1410483989
Entrez Id: 8826
Gene Symbol: IQGAP1
IQGAP1
CUI: C3489532
Disease:
Cone-Rod Dystrophy 2
0.010 GeneticVariation BEFREE Finally, genotype-phenotype correlation is not obvious in our cohort with CRD; even if, the Canadian subjects with the allele 409G>A had a more severe degree (P<0.001) of hypocholesterolemia than the other patients, many clinical data are inconsistent with a hypothetical genotype-phenotype correlation. 19285442 2009