Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10800309 0.925 0.120 1 161502368 upstream gene variant A/G;T snv 3
rs11010067 0.925 0.040 10 35006503 downstream gene variant C/G snv 0.37 3
rs113010081 0.925 0.160 3 46415921 downstream gene variant T/C snv 7.3E-02 3
rs11742570 0.925 0.040 5 40410482 upstream gene variant T/C;G snv 3
rs17694108 0.925 0.040 19 33240645 regulatory region variant G/A snv 0.22 3
rs2097432 1.000 0.040 6 32622994 TF binding site variant T/C snv 0.27 3
rs2413583 0.925 0.040 22 39263768 intron variant C/T snv 0.19 3
rs4286721 1.000 0.040 5 40497502 intron variant G/A snv 0.64 3
rs4409764 0.925 0.040 10 99524480 upstream gene variant T/A;G snv 3
rs75900472 0.925 0.040 9 4981601 upstream gene variant CC/A;C delins 4.6E-02 3
rs10051722 1.000 0.040 5 130768383 intron variant A/C;G snv 2
rs10500264 1.000 0.080 19 33259408 intergenic variant G/A snv 0.14 2
rs11195128 1.000 0.040 10 110426390 downstream gene variant C/G;T snv 2
rs11554257 1.000 0.040 9 114842790 upstream gene variant T/C snv 0.13 2
rs11672983 1.000 0.040 19 54871595 upstream gene variant G/A snv 0.35 2
rs11734570 1.000 0.040 4 38586832 intergenic variant G/A snv 0.39 2
rs11739135 1.000 0.040 5 132397705 downstream gene variant G/C snv 0.27 2
rs117829974 1.000 0.040 3 62886233 intergenic variant C/A;G;T snv 2
rs117927258 1.000 0.080 6 47108781 intergenic variant T/C snv 2.6E-04 2
rs11969064 6 18104864 intergenic variant C/T snv 0.11 2
rs12627970 1.000 0.080 22 39325740 TF binding site variant A/G snv 0.19 2
rs13204742 1.000 0.040 6 127924620 intergenic variant G/T snv 9.3E-02 2
rs145080284 1.000 0.080 10 94662973 intergenic variant C/G snv 2.8E-02 2
rs1505992 5 40498475 intron variant A/T snv 0.61 2
rs16940202 1.000 0.040 16 85980635 intron variant T/C snv 0.15 2