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: rs1801394
rs1801394
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.100 0.900 10 2003 2018
dbSNP: rs1532268
rs1532268
0.776 0.280 5 7878066 missense variant C/T snv 0.31 0.32
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.030 1.000 3 2011 2018
dbSNP: rs326119
rs326119
0.925 0.120 5 7869970 intron variant C/A;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.020 1.000 2 2012 2015
dbSNP: rs372359132
rs372359132
0.827 0.160 5 7878203 missense variant A/G snv 4.0E-06 2.1E-05
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2012 2012