Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397514735
rs397514735
DNM2
0.800 GeneticVariation UNIPROT Dynamin 2 homozygous mutation in humans with a lethal congenital syndrome. 23092955

2013
dbSNP: rs397514735
rs397514735
DNM2
G 0.800 CausalMutation CLINVAR