Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs372958987
rs372958987
EDN3
0.010 GeneticVariation BEFREE Therefore, we conclude that S390R and C109R mutations could cause HSCR but that N104I mutation might be polymorphous. 9556633

1998