Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12593813
rs12593813
Entrez Id: 5607
Gene Symbol: MAP2K5
MAP2K5
CUI: C0035258
Disease:
Restless Legs Syndrome
0.810 GeneticVariation BEFREE However, the haplotype analysis showed that the G-G-G-G-T (rs1026732-rs11635424-rs12593813-rs4489954-rs3784709) haplotype was associated with RLS symptoms (permutation p=0.033). 29422930 2018
dbSNP: rs12593813
rs12593813
Entrez Id: 5607
Gene Symbol: MAP2K5
MAP2K5
CUI: C0035258
Disease:
Restless Legs Syndrome
G 0.810 GeneticVariation GWASDB Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1. 21779176 2011
dbSNP: rs12593813
rs12593813
Entrez Id: 5607
Gene Symbol: MAP2K5
MAP2K5
CUI: C0035258
Disease:
Restless Legs Syndrome
G 0.810 GeneticVariation GWASCAT Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1. 21779176 2011
dbSNP: rs12593813
rs12593813
Entrez Id: 5607
Gene Symbol: MAP2K5
MAP2K5
CUI: C0035258
Disease:
Restless Legs Syndrome
G 0.810 GeneticVariation GWASCAT Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. 17637780 2007
dbSNP: rs12593813
rs12593813
Entrez Id: 5607
Gene Symbol: MAP2K5
MAP2K5
CUI: C0035258
Disease:
Restless Legs Syndrome
G 0.810 GeneticVariation GWASDB Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. 17637780 2007
dbSNP: rs1026732
rs1026732
Entrez Id: 5607
Gene Symbol: MAP2K5
MAP2K5
CUI: C0035258
Disease:
Restless Legs Syndrome
0.720 GeneticVariation BEFREE However, the haplotype analysis showed that the G-G-G-G-T (rs1026732-rs11635424-rs12593813-rs4489954-rs3784709) haplotype was associated with RLS symptoms (permutation p=0.033). 29422930 2018
dbSNP: rs1026732
rs1026732
Entrez Id: 5607
Gene Symbol: MAP2K5
MAP2K5
CUI: C0035258
Disease:
Restless Legs Syndrome
0.720 GeneticVariation BEFREE Case-control association studies showed significant association between all three variants and RLS (P=0.0001/OR=1.65, P=0.0021/OR=1.59, and P=0.0011/OR=1.55 for rs2300478, rs9357271, and rs1026732, respectively). 21925394 2011
dbSNP: rs1026732
rs1026732
Entrez Id: 5607
Gene Symbol: MAP2K5
MAP2K5
CUI: C0035258
Disease:
Restless Legs Syndrome
0.720 GeneticVariation GWASDB Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. 17637780 2007
dbSNP: rs11635424
rs11635424
Entrez Id: 5607
Gene Symbol: MAP2K5
MAP2K5
CUI: C0035258
Disease:
Restless Legs Syndrome
0.710 GeneticVariation BEFREE However, the haplotype analysis showed that the G-G-G-G-T (rs1026732-rs11635424-rs12593813-rs4489954-rs3784709) haplotype was associated with RLS symptoms (permutation p=0.033). 29422930 2018
dbSNP: rs3784709
rs3784709
Entrez Id: 5607
Gene Symbol: MAP2K5
MAP2K5
CUI: C0035258
Disease:
Restless Legs Syndrome
0.710 GeneticVariation BEFREE However, the haplotype analysis showed that the G-G-G-G-T (rs1026732-rs11635424-rs12593813-rs4489954-rs3784709) haplotype was associated with RLS symptoms (permutation p=0.033). 29422930 2018
dbSNP: rs4489954
rs4489954
Entrez Id: 5607
Gene Symbol: MAP2K5
MAP2K5
CUI: C0035258
Disease:
Restless Legs Syndrome
0.710 GeneticVariation BEFREE However, the haplotype analysis showed that the G-G-G-G-T (rs1026732-rs11635424-rs12593813-rs4489954-rs3784709) haplotype was associated with RLS symptoms (permutation p=0.033). 29422930 2018
dbSNP: rs11635424
rs11635424
Entrez Id: 5607
Gene Symbol: MAP2K5
MAP2K5
CUI: C0035258
Disease:
Restless Legs Syndrome
0.710 GeneticVariation GWASDB Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. 17637780 2007
dbSNP: rs3784709
rs3784709
Entrez Id: 5607
Gene Symbol: MAP2K5
MAP2K5
CUI: C0035258
Disease:
Restless Legs Syndrome
0.710 GeneticVariation GWASDB Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. 17637780 2007
dbSNP: rs4489954
rs4489954
Entrez Id: 5607
Gene Symbol: MAP2K5
MAP2K5
CUI: C0035258
Disease:
Restless Legs Syndrome
0.710 GeneticVariation GWASDB Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. 17637780 2007
dbSNP: rs868036
rs868036
Entrez Id: 5607
Gene Symbol: MAP2K5
MAP2K5
CUI: C0035258
Disease:
Restless Legs Syndrome
A 0.700 GeneticVariation GWASCAT Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis. 29029846 2017
dbSNP: rs41305272
rs41305272
Entrez Id: 5607
Gene Symbol: MAP2K5
MAP2K5
CUI: C0035258
Disease:
Restless Legs Syndrome
0.010 GeneticVariation BEFREE A predicted miR-330-3p target site SNP (rs41305272) in mitogen-activated protein kinase kinase 5 (MAP2K5) mRNA was in LD (d' = 1.0, r(2) = 0.02) with a reported GWAS-identified variant for restless legs syndrome (RLS), a disorder frequently comorbid with anxiety and depression, possibly because of a shared pathophysiology. 24436253 2014