Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs11584383
MROH3P
0.827 0.200 1 200966738 downstream gene variant T/C snv 0.24 4
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 3
rs13192471 0.925 0.160 6 32703326 downstream gene variant T/C snv 0.19 3
rs6478106 0.925 0.080 9 114783386 downstream gene variant C/T snv 0.34 2
rs9988642
IL23R
0.882 0.080 1 67260421 downstream gene variant T/C snv 0.13 2
rs10789230 1.000 0.040 1 67264945 downstream gene variant G/C;T snv 1
rs11010067 0.925 0.040 10 35006503 downstream gene variant C/G snv 0.37 1
rs11195128 1.000 0.040 10 110426390 downstream gene variant C/G;T snv 1
rs12567232 1.000 0.040 1 67262335 downstream gene variant G/A snv 0.27 1
rs12946510 0.851 0.160 17 39756124 downstream gene variant C/T snv 0.37 1
rs281379 1.000 0.040 19 48711017 downstream gene variant G/A snv 0.38 1
rs3091338 1.000 0.040 5 132067045 downstream gene variant C/T snv 0.30 1
rs3897478 1.000 0.040 1 119908567 downstream gene variant T/C snv 0.17 1
rs6669582 1.000 0.040 1 67264372 downstream gene variant A/G snv 0.35 1
rs7186163 1.000 0.040 16 50652646 downstream gene variant A/C snv 0.63 1
rs7539328 1.000 0.040 1 67266920 downstream gene variant G/A;T snv 1
rs8050932 1.000 0.040 16 50653762 downstream gene variant C/T snv 0.66 1
rs806438
SPACA1
1.000 0.040 6 88067263 downstream gene variant T/A;C;G snv 1
rs991804 1.000 0.040 17 34260706 downstream gene variant C/T snv 0.33 1
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 9
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 7
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6