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: rs1454626
rs1454626
9 2621030 intron variant C/A snv 0.66
CUI: C0007273
Disease: Carotid Artery Diseases
Carotid Artery Diseases
Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2008 2008