Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10401672 19 33269055 regulatory region variant C/T snv 0.30 1
rs113721499 6 31261530 intergenic variant C/T snv 1
rs12748961 1 205707135 intergenic variant T/C snv 0.12 1
rs150876292 11 69874913 regulatory region variant T/C snv 5.1E-04 1
rs1537061 1 87273536 regulatory region variant T/C snv 0.14 1
rs171835 6 81755270 upstream gene variant G/A snv 0.26 1
rs200830364 11 90199744 downstream gene variant AAAAA/-;A;AA;AAA;AAAA;AAAAAA delins 0.38 1
rs28479481 14 23123308 upstream gene variant C/T snv 5.5E-02 1
rs2921071 8 8450534 regulatory region variant A/C;G snv 1
rs2980884 8 125462114 upstream gene variant G/A snv 0.49 1
rs34129834 19 33264533 intergenic variant T/C snv 0.29 1
rs34610286 19 33263765 TF binding site variant G/T snv 0.11 1
rs550065584 9 132999365 intergenic variant G/A snv 8.0E-04 1
rs56757486 19 836144 upstream gene variant G/A snv 0.19 1
rs6703781 1 87283202 intergenic variant G/A snv 0.14 1
rs6782812 3 128599154 intergenic variant G/A snv 0.89 1
rs70992176 2 147841722 upstream gene variant A/- delins 1
rs71560490 7 75831253 upstream gene variant G/A snv 0.10 1
rs7253959 19 33264178 intergenic variant G/A;C snv 1
rs7315361 12 66277999 upstream gene variant T/A snv 0.44 1
rs75497452 2 212858270 intron variant C/A;T snv 1
rs79565040 1 8857339 downstream gene variant -/AT delins 0.43 1
rs9376098 6 135178322 upstream gene variant T/A snv 0.44 1
rs9743723 14 23107989 upstream gene variant C/G;T snv 1
rs924135
ABCC1
16 16029602 intron variant A/C;T snv 1