rs1137100, LEPR

N. diseases: 39
Disease: HELLP Syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
HELLP Syndrome
CUI: C0162739
Disease: HELLP Syndrome
0.010 GeneticVariation BEFREE However the LEPR c.326A>G AG genotype was twice more frequent and the (AG AG GG AG) haplotype was three times more frequent in HELLP syndrome patients. 20149225 2010