Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs139604259
MACO1
1 25442718 intron variant -/A delins 0.58 1
rs66883945 6 138996690 regulatory region variant -/C;CC delins 1
rs112959129
ABHD11-AS1
7 73733661 upstream gene variant -/CA delins 1
rs201445483
SMC6
2 17708820 intron variant -/GT delins 7.3E-05 2
rs3832016
CELSR2
1 109275536 3 prime UTR variant -/T ins 0.74 1
rs68055275
ST3GAL4
11 126369248 intron variant -/T;TT delins 3
rs34774090
SPC24
19 11143211 intron variant A/- delins 0.77 1
rs145955280
EVI5
1 92671973 intron variant A/-;AA;AAA delins 2
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs174574
FADS2
1.000 0.080 11 61832870 intron variant A/C snv 0.55 5
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 5
rs1797912
PPARG
1.000 0.040 3 12428740 intron variant A/C snv 0.33 2
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 2
rs496800 1 234715469 intron variant A/C snv 0.65 2
rs557933 1 234717521 intron variant A/C snv 0.65 2
rs74551598
WHRN
9 114415286 intron variant A/C snv 0.20 2
rs201148465
H1-5
6 27867515 synonymous variant A/C snv 1.9E-04 1.7E-04 1
rs2294261 6 16108932 downstream gene variant A/C snv 0.65 1
rs585967 1.000 0.040 2 21047682 upstream gene variant A/C snv 0.81 1
rs72653060
APOB
2 21034825 missense variant A/C snv 9.9E-05 5.0E-04 1
rs7873387
ABCA1
9 104833321 intron variant A/C snv 0.20 1
rs826682
LIMS1
2 108615932 intron variant A/C snv 0.18 1
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 5
rs77960347
LIPG
18 49583585 missense variant A/C;G snv 4.0E-06; 8.7E-03 5
rs11207995
DOCK7
1 62583880 intron variant A/C;G snv 3