Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs41291957
rs41291957
MIR143 ; MIR145 ; CARMN
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease 		0.010 GeneticVariation BEFREE Therefore, the authors hypothesized that rs41291957 in pri-miR-143 might be involved in the risk of sporadic congenital heart disease (CHD). 24752771

2014