Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906962
rs387906962
MRPL3
0.800 GeneticVariation UNIPROT Exome sequencing identifies MRPL3 mutation in mitochondrial cardiomyopathy. 21786366

2011
dbSNP: rs387906962
rs387906962
MRPL3
C 0.800 CausalMutation CLINVAR