Source: BEFREE

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: rs5742904
rs5742904
APOB
0.689 0.280 2 21006288 missense variant C/A;T snv 2.8E-04 7.3E-04
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.020 1.000 2 2001 2001
dbSNP: rs1042034
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.010 1.000 1 2013 2013
dbSNP: rs676210
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.010 1.000 1 2014 2014
dbSNP: rs693
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.010 1.000 1 2018 2018