Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11004733 0.882 0.040 10 55089584 intron variant C/T snv 2.9E-02 4
rs141252918 0.882 0.040 6 151506923 intron variant G/A;C snv 4
rs149268645 0.882 0.040 2 202968295 intron variant G/A snv 8.4E-02 4
rs4870888 0.882 0.040 8 124096736 intron variant T/C snv 0.39 4
rs62173322 0.882 0.040 2 169754519 intron variant A/G snv 0.32 4
rs76371172 0.882 0.040 15 31522252 intron variant T/G snv 9.1E-03 4
rs9577511 0.882 0.040 13 113337508 intron variant A/G snv 0.15 4
rs17173608 0.807 0.240 7 150339575 intron variant T/G snv 0.11 3
rs17387100 0.925 0.040 4 15993502 intron variant A/G snv 7.5E-02 3
rs26318 0.925 0.040 5 116352208 intron variant C/T snv 0.99 3
rs300774 0.925 0.040 2 112496 intergenic variant A/C;T snv 2
rs7296262 1.000 0.040 12 128610527 intron variant T/C;G snv 2