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: rs387906691
rs387906691
TBXA2R
1.000 19 3595810 missense variant C/T snv
CUI: C3279614
Disease: BLEEDING DISORDER, PLATELET-TYPE, 13, SUSCEPTIBILITY TO
BLEEDING DISORDER, PLATELET-TYPE, 13, SUSCEPTIBILITY TO 		0.700 0
dbSNP: rs387906691
rs387906691
TBXA2R
1.000 19 3595810 missense variant C/T snv
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders 		0.010 1.000 1 2010 2010