Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 8
rs1746048 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 3
rs17630235
TRAFD1
0.925 0.120 12 112153882 downstream gene variant G/A;C snv 3
rs2967605
RAB11B
0.925 0.040 19 8404854 downstream gene variant C/T snv 0.20 3
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 3
rs7395662 0.882 0.080 11 48497341 downstream gene variant A/G snv 0.56 3
rs2066865
FGG
0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 2
rs2814944 1.000 0.040 6 34585020 downstream gene variant G/A snv 0.20 2
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 2
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 1
rs1746049 1.000 0.040 10 44280862 downstream gene variant C/T snv 0.23 1
rs3931020 0.882 0.040 1 74769633 downstream gene variant T/C snv 0.71 1
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 1
rs535949 1.000 0.040 10 44256882 downstream gene variant G/T snv 0.24 1
rs671765 1.000 0.040 10 44257528 downstream gene variant A/G;T snv 1
rs687175 1.000 0.040 10 44256462 downstream gene variant T/C snv 0.24 1
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 8
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 7
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 6
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 6
rs6882076
TIMD4
0.827 0.160 5 156963286 upstream gene variant T/C snv 0.56 4