Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs16841013
rs16841013
LMX1A ; LMX1A-AS2
0.010 GeneticVariation BEFREE Genotypic frequencies of 3 SNPs at rs6671290, rs1354510, and r</span>s16841013 were found to exhibit significant differences between patients with CS with failure of formation and the healthy controls (P = 0.019, 0.007, and 0.006, respectively). 25099324

2014