ANK2, ankyrin 2, 287

N. diseases: 71; N. variants: 37
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121912705
rs121912705
Entrez Id: 287
Gene Symbol: ANK2
ANK2
CUI: C1970119
Disease:
CARDIAC ARRHYTHMIA, ANKYRIN-B-RELATED 		0.800 GeneticVariation UNIPROT Ankyrin-B syndrome: enhanced cardiac function balanced by risk of cardiac death and premature senescence. 17940615 2007
dbSNP: rs121912705
rs121912705
Entrez Id: 287
Gene Symbol: ANK2
ANK2
CUI: C1970119
Disease:
CARDIAC ARRHYTHMIA, ANKYRIN-B-RELATED 		0.800 GeneticVariation UNIPROT A cardiac arrhythmia syndrome caused by loss of ankyrin-B function. 15178757 2004
dbSNP: rs121912705
rs121912705
Entrez Id: 287
Gene Symbol: ANK2
ANK2
CUI: C1970119
Disease:
CARDIAC ARRHYTHMIA, ANKYRIN-B-RELATED 		0.800 GeneticVariation UNIPROT Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death. 12571597 2003
dbSNP: rs121912705
rs121912705
Entrez Id: 287
Gene Symbol: ANK2
ANK2
CUI: C1970119
Disease:
CARDIAC ARRHYTHMIA, ANKYRIN-B-RELATED 		A 0.800 CausalMutation CLINVAR
dbSNP: rs29356
rs29356
Entrez Id: 287
Gene Symbol: ANK2
ANK2
CUI: C0428883
Disease:
Diastolic blood pressure 		T 0.700 GeneticVariation GWASCAT A genome-wide association and replication study of blood pressure in Ugandan early adolescents. 31469255 2019
dbSNP: rs41496644
rs41496644
Entrez Id: 287
Gene Symbol: ANK2
ANK2
CUI: C1861172
Disease:
Venous Thromboembolism 		0.700 GeneticVariation GWASCAT Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism. 31420334 2019
dbSNP: rs17045918
rs17045918
Entrez Id: 287
Gene Symbol: ANK2
ANK2
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs17045918
rs17045918
Entrez Id: 287
Gene Symbol: ANK2
ANK2
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs34311906
rs34311906
Entrez Id: 287
Gene Symbol: ANK2
ANK2
CUI: C0948008
Disease:
Ischemic stroke 		0.700 GeneticVariation GWASCAT Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. 29531354 2018
dbSNP: rs34311906
rs34311906
Entrez Id: 287
Gene Symbol: ANK2
ANK2
CUI: C0038454
Disease:
Cerebrovascular accident 		0.700 GeneticVariation GWASCAT Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. 29531354 2018
dbSNP: rs10011263
rs10011263
Entrez Id: 287
Gene Symbol: ANK2
ANK2
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: rs11098185
rs11098185
Entrez Id: 287;105377373
Gene Symbol: ANK2;ANK2-AS1
ANK2;ANK2-AS1
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: rs11098185
rs11098185
Entrez Id: 287;105377373
Gene Symbol: ANK2;ANK2-AS1
ANK2;ANK2-AS1
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: rs11723518
rs11723518
Entrez Id: 287
Gene Symbol: ANK2
ANK2
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: rs11728431
rs11728431
Entrez Id: 287
Gene Symbol: ANK2
ANK2
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: rs17044897
rs17044897
Entrez Id: 287
Gene Symbol: ANK2
ANK2
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: rs17044925
rs17044925
Entrez Id: 287
Gene Symbol: ANK2
ANK2
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: rs17045462
rs17045462
Entrez Id: 287;105377373
Gene Symbol: ANK2;ANK2-AS1
ANK2;ANK2-AS1
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: rs17607420
rs17607420
Entrez Id: 287
Gene Symbol: ANK2
ANK2
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: rs199473346
rs199473346
Entrez Id: 287
Gene Symbol: ANK2
ANK2
CUI: C1970119
Disease:
CARDIAC ARRHYTHMIA, ANKYRIN-B-RELATED 		A 0.700 GeneticVariation CLINVAR A subtype of idiopathic ventricular fibrillation and its relevance to catheter ablation and genetic variants. 28736713 2017
dbSNP: rs4364265
rs4364265
Entrez Id: 287
Gene Symbol: ANK2
ANK2
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: rs4626206
rs4626206
Entrez Id: 287
Gene Symbol: ANK2
ANK2
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: rs5022543
rs5022543
Entrez Id: 287
Gene Symbol: ANK2
ANK2
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: rs6828678
rs6828678
Entrez Id: 287
Gene Symbol: ANK2
ANK2
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: rs6829775
rs6829775
Entrez Id: 287
Gene Symbol: ANK2
ANK2
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