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: rs1994016
rs1994016
0.851 0.160 15 78787892 intron variant C/T snv 0.30
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs3825807
rs3825807
0.807 0.120 15 78796769 missense variant A/G snv 0.34 0.33
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
Cardiovascular Diseases 0.010 1.000 1 2018 2018