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: rs2070744
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.050 1.000 5 2013 2019