rs778686781, PLG

N. diseases: 1
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Dysfibrinogenemia
CUI: C1260903
Disease: Dysfibrinogenemia
6 1.000 0.080 6 160718329 missense variant T/C snv 4.0E-06 0.010 1.000 1 2000 2000