THBS2, thrombospondin 2, 7058

N. diseases: 149; N. variants: 13
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: rs761646500
rs761646500
0.925 0.080 6 169237763 missense variant C/G snv 4.0E-06
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.020 1.000 2 2002 2015
dbSNP: rs8089
rs8089
0.851 0.080 6 169217631 splice region variant A/C snv 0.22
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 < 0.001 1 2011 2011