Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 7
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 8
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 6
rs505151
PCSK9
0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 3
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 6
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 1
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 2
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs585967 1.000 0.040 2 21047682 upstream gene variant A/C snv 0.81 3
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 8
rs2227564
PLAU ; C10orf55
0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 1
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 1
rs606452
SERPINH1
1.000 0.040 11 75565133 intron variant A/C snv 0.78 1
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 5
rs1250229 1.000 0.040 2 215439661 upstream gene variant T/C snv 0.77 2
rs6544713
ABCG8
0.925 0.040 2 43846742 non coding transcript exon variant T/C snv 0.75 5
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs515135 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 6
rs644045
CYP21A2 ; C2
0.851 0.240 6 31916180 intron variant A/G snv 0.72 2
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 3
rs3931020 0.882 0.040 1 74769633 downstream gene variant T/C snv 0.71 1
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 7
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 1
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 1