Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs34377097
rs34377097
TBXA2R
1.000 19 3600456 missense variant C/A snv 5.8E-05 2.1E-05
CUI: C3279614
Disease: BLEEDING DISORDER, PLATELET-TYPE, 13, SUSCEPTIBILITY TO
BLEEDING DISORDER, PLATELET-TYPE, 13, SUSCEPTIBILITY TO 		0.800 1.000 2 1994 1996
dbSNP: rs34377097
rs34377097
TBXA2R
1.000 19 3600456 missense variant C/A snv 5.8E-05 2.1E-05
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders 		0.010 1.000 1 1994 1994