Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4646342
rs4646342
Entrez Id: 10400
Gene Symbol: PEMT
PEMT
CUI: C0205682
Disease:
Waist-Hip Ratio 		A 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs8078513
rs8078513
Entrez Id: 10400
Gene Symbol: PEMT
PEMT
CUI: C0205682
Disease:
Waist-Hip Ratio 		A 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs7946
rs7946
Entrez Id: 10400
Gene Symbol: PEMT
PEMT
CUI: C4529962
Disease:
Fatty Liver Disease 		0.020 GeneticVariation BEFREE Decreased liver PC content in individuals with the NASH is independent of PEMT V175M genotype and could be partly linked to decreased GNMT expression. 31199045 2019
dbSNP: rs1109859
rs1109859
Entrez Id: 10400
Gene Symbol: PEMT
PEMT
CUI: C0028754
Disease:
Obesity 		0.010 GeneticVariation BEFREE One hundred ninety-six children with obesity (101 females, 95 males) were evaluated using anthropometric measurements, dietary intakes, plasma and RBC PUFA quantification, blood biochemistry, and 55 single nucleotide polymorphisms within 14 genes. phosphatidylethanolamine <i>N</i>-methyltransferase (<i>PEMT</i>) rs1109859 and methylenetetrahydrofolate reductase gene (<i>MTHFR</i>) rs4846052 genotypes were associated with PUFA levels in RBCs. 31671528 2019