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