C5, complement C5, 727

N. diseases: 129; N. variants: 20
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: rs1035029
rs1035029
1.000 0.040 9 120980540 intron variant G/A snv 0.63
CUI: C0031099
Disease: Periodontitis
Periodontitis
Stomatognathic Diseases 0.010 1.000 1 2010 2010
dbSNP: rs17611
rs17611
0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36
CUI: C0031099
Disease: Periodontitis
Periodontitis
Stomatognathic Diseases 0.010 1.000 1 2010 2010
dbSNP: rs25681
rs25681
0.882 0.120 9 121017727 synonymous variant G/A snv 0.47 0.35
CUI: C0031099
Disease: Periodontitis
Periodontitis
Stomatognathic Diseases 0.010 1.000 1 2010 2010
dbSNP: rs992670
rs992670
0.882 0.120 9 121019492 intron variant G/A snv 0.52
CUI: C0031099
Disease: Periodontitis
Periodontitis
Stomatognathic Diseases 0.010 1.000 1 2010 2010