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: rs1333049
rs1333049
0.614 0.520 9 22125504 intron variant G/C snv 0.41
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.800 1.000 1 2011 2013
dbSNP: rs1537370
rs1537370
1.000 9 22084311 intron variant C/T snv 0.55
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.800 1.000 1 2011 2013