Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137852769
rs137852769
HADHA ; GAREM2
0.020 GeneticVariation BEFREE Neither maternal nor fetal heterozygosity for the E474Q mutation is a relevant factor of HELLP syndrome. 17313315

2007
dbSNP: rs137852769
rs137852769
HADHA ; GAREM2
0.020 GeneticVariation BEFREE While carrying fetuses with the Glu474Gln mutation, 79 percent of the heterozygous mothers had fatty liver of pregnancy or the HELLP syndrome. 10352164

1999