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: rs150629733
rs150629733
0.851 0.080 3 148741190 missense variant T/C;G snv 4.0E-06; 8.8E-05
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
Cardiovascular Diseases 0.010 1.000 1 1999 1999
dbSNP: rs3772622
rs3772622
0.851 0.080 3 148717966 intron variant T/A;C snv
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs5182
rs5182
0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
Cardiovascular Diseases 0.010 < 0.001 1 1994 1994
dbSNP: rs5186
rs5186
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs553350297
rs553350297
0.882 0.040 3 148741588 missense variant G/A snv 1.2E-05 2.1E-05
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
Cardiovascular Diseases 0.010 1.000 1 1999 1999