CR2, complement C3d receptor 2, 1380

N. diseases: 123; N. variants: 9
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs17615
rs17615
0.827 0.200 1 207473117 missense variant G/A snv 0.26 0.31
CUI: C0032285
Disease: Pneumonia
Pneumonia
Infections; Respiratory Tract Diseases 0.010 1.000 1 2018 2018
dbSNP: rs17616
rs17616
1.000 0.080 1 207473578 missense variant G/A snv 0.26 0.30
CUI: C0032285
Disease: Pneumonia
Pneumonia
Infections; Respiratory Tract Diseases 0.010 1.000 1 2018 2018
dbSNP: rs4308977
rs4308977
0.925 0.160 1 207473553 missense variant T/A;C snv 4.0E-06; 0.27
CUI: C0032285
Disease: Pneumonia
Pneumonia
Infections; Respiratory Tract Diseases 0.010 1.000 1 2018 2018