Disease: HELLP Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137852769
rs137852769
Entrez Id: 3030;150946
Gene Symbol: HADHA;GAREM2
HADHA;GAREM2
CUI: C0162739
Disease:
HELLP Syndrome 		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
Entrez Id: 3030;150946
Gene Symbol: HADHA;GAREM2
HADHA;GAREM2
CUI: C0162739
Disease:
HELLP Syndrome 		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