Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs565224393
rs565224393
NARS2
T 0.700 GeneticVariation CLINVAR Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome. 25807530

2015
dbSNP: rs565224393
rs565224393
NARS2
T 0.700 CausalMutation CLINVAR