Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1684041 15 64908605 intron variant C/T snv 0.19 1
rs17655730 11 270715 intergenic variant T/C snv 0.20 1
rs185523698 20 58977406 intron variant C/T snv 1.6E-02 1
rs2113036 19 16106643 upstream gene variant T/C snv 0.28 1
rs2138852 17 29376331 intron variant C/G;T snv 1
rs236907 1 171675446 upstream gene variant G/A snv 0.15 1
rs2546976 5 160173207 intergenic variant T/C snv 0.70 1
rs2950390 12 56661507 downstream gene variant C/G;T snv 1
rs3131057 6 30794316 downstream gene variant T/C snv 0.61 1
rs35304300 6 139536204 intron variant A/G snv 0.15 1
rs35547687 7 158833186 upstream gene variant -/A;AA delins 1
rs4812048 20 59012716 intergenic variant C/T snv 0.15 1
rs528863805 16 29855475 downstream gene variant T/-;TT;TTT delins 1
rs56990409 12 7989603 intergenic variant -/A;AA;AAAAAAA delins 1
rs57567837 13 113370553 intergenic variant T/C snv 3.5E-02 1
rs6099612 20 57411745 downstream gene variant A/G snv 0.16 1
rs6446731 4 3283024 regulatory region variant G/A snv 0.38 1
rs6759839 2 16439535 intergenic variant A/G snv 0.56 1
rs6805910 3 56705895 intergenic variant T/C snv 0.56 1
rs6992820 8 55851897 TF binding site variant A/G;T snv 1
rs7225537 17 17009366 downstream gene variant C/A;G;T snv 1
rs7249578 19 35171354 downstream gene variant G/A snv 0.37 1
rs72669198 4 122595396 intergenic variant T/C snv 9.4E-03 1
rs7596219 2 66415818 intergenic variant A/G snv 0.14 1
rs779314480 20 59010966 upstream gene variant TTTTTTT/-;T;TT;TTT;TTTT;TTTTT;TTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTTTTTTTTT delins 1