Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1469513
APOB
1.000 0.080 2 21036690 intron variant T/C snv 0.34 1
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 7
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 3
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 7
rs5742904
APOB
0.689 0.280 2 21006288 missense variant C/A;T snv 2.8E-04 7.3E-04 3
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 7