rs34377097, TBXA2R

N. diseases: 2
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.
BLEEDING DISORDER, PLATELET-TYPE, 13, SUSCEPTIBILITY TO
CUI: C3279614
Disease: BLEEDING DISORDER, PLATELET-TYPE, 13, SUSCEPTIBILITY TO
3 1.000 19 3600456 missense variant C/A snv 5.8E-05 2.1E-05 0.800 1.000 2 1994 1996
Blood Coagulation Disorders
CUI: C0005779
Disease: Blood Coagulation Disorders
31 1.000 19 3600456 missense variant C/A snv 5.8E-05 2.1E-05 0.010 1.000 1 1994 1994