Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9296249
rs9296249
BTBD9
0.820 GeneticVariation BEFREE Moreover, we found the haplotype polymorphisms of rs9357271, rs3923809, and rs9296249 (overall p=5.69×10<sup>-18</sup>) in <i>BTBD9</i> was associated with RLS. 29209388

2017
dbSNP: rs9296249
rs9296249
BTBD9
0.820 GeneticVariation BEFREE A further meta-analysis of RLS in Asian population found that two SNPs of BTBD9 increased the risk of RLS: rs9296249 of BTBD9 (OR = 1.44, p = .000, T allele), rs9357271 of BTBD9 (OR = 1.38, p = .021, dominant model). 28329290

2017
dbSNP: rs9296249
rs9296249
BTBD9
T 0.820 GeneticVariation GWASCAT Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. 17637780

2007
dbSNP: rs9296249
rs9296249
BTBD9
T 0.820 GeneticVariation GWASDB Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. 17637780

2007