Have questions? Visit https://www.reddit.com/r/SNPedia

rs398123091(A;G)

From SNPedia
Carrier of a VLCAD deficiency mutation
Is agenotype
ofrs398123091
GeneACADVL, DLG4
Chromosome17
Position7,221,993
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(A;G) 3 Carrier of a VLCAD deficiency mutation
(G;G) 0 common in clinvar

Unaffected in absence of a second ACADVL gene mutation