Gene: LRP2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4036
Gene Symbol: LRP2
LRP2 		0.010 Biomarker group BEFREE A missense mutation in <i>TCN2</i> is associated with decreased risk for congenital heart defects and may increase cellular uptake of vitamin B12 via Megalin. 28903415 2017