Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs773677327
rs773677327
ACADM
G 0.700 GeneticVariation CLINVAR [An analysis of clinical characteristics and gene mutation in two patients with medium- and short-chain acyl-CoA dehydrogenase deficiency]. 27751224

2016
dbSNP: rs773677327
rs773677327
ACADM
G 0.700 CausalMutation CLINVAR [An analysis of clinical characteristics and gene mutation in two patients with medium- and short-chain acyl-CoA dehydrogenase deficiency]. 27751224

2016
dbSNP: rs773677327
rs773677327
ACADM
G 0.700 CausalMutation CLINVAR Fatty Acid oxidation disorders in a chinese population in taiwan. 23700290

2013
dbSNP: rs773677327
rs773677327
ACADM
G 0.700 GeneticVariation CLINVAR Fatty Acid oxidation disorders in a chinese population in taiwan. 23700290

2013
dbSNP: rs773677327
rs773677327
ACADM
G 0.700 CausalMutation CLINVAR Allelic diversity in MCAD deficiency: the biochemical classification of 54 variants identified during 5 years of ACADM sequencing. 20434380

2010
dbSNP: rs773677327
rs773677327
ACADM
G 0.700 GeneticVariation CLINVAR Allelic diversity in MCAD deficiency: the biochemical classification of 54 variants identified during 5 years of ACADM sequencing. 20434380

2010
dbSNP: rs773677327
rs773677327
ACADM
G 0.700 GeneticVariation CLINVAR Novel mutations causing medium chain acyl-CoA dehydrogenase deficiency: under-representation of the common c.985 A > G mutation in the New York state population. 18241067

2008
dbSNP: rs773677327
rs773677327
ACADM
G 0.700 CausalMutation CLINVAR Novel mutations causing medium chain acyl-CoA dehydrogenase deficiency: under-representation of the common c.985 A > G mutation in the New York state population. 18241067

2008