Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4744899 1.000 0.040 9 69461631 non coding transcript exon variant A/G snv 0.55 2
rs6559648 0.925 0.040 9 69594728 intron variant T/A snv 3.2E-02 2
rs11138902 9 69488398 intron variant G/A;T snv 1
rs1105307 9 69431124 3 prime UTR variant G/A snv 0.32 1
rs7033137 9 69440242 intron variant C/G;T snv 1
rs7049022 9 69440259 intron variant A/G snv 0.20 1
rs7859472 9 69490489 intron variant T/A snv 0.78 1
rs11138947 9 69495646 intron variant C/T snv 0.71 1