Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2981582 0.695 0.360 10 121592803 intron variant A/G snv 0.58 20
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 20
rs744166 0.689 0.560 17 42362183 intron variant A/G snv 0.48 20
rs2267437 0.724 0.320 22 41620695 intron variant C/A;G snv 19
rs6010620 0.701 0.360 20 63678486 intron variant A/C;G snv 19
rs7804372 0.716 0.320 7 116554174 intron variant T/A snv 0.27 19
rs10165970 0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs10519097 0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs11943456 0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs17024869 0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs352139 0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 18
rs7581886 0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs13281615 0.716 0.360 8 127343372 intron variant A/G snv 0.43 17
rs1412125 0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs2069837 0.724 0.520 7 22728408 intron variant A/C;G snv 17
rs3802842 0.695 0.280 11 111300984 intron variant C/A snv 0.71 17
rs3807987 0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 17
rs1219648 0.716 0.320 10 121586676 intron variant A/G;T snv 16
rs12203592 0.649 0.320 6 396321 intron variant C/T snv 0.10 16
rs16901979 0.724 0.480 8 127112671 intron variant C/A snv 0.16 16
rs17251221 0.724 0.360 3 122274400 intron variant A/G snv 0.11 16
rs2107425 0.732 0.280 11 1999845 intron variant C/T snv 16
rs4939827 0.708 0.160 18 48927093 intron variant T/A;C snv 16
rs8175347 0.708 0.400 2 233760234 intron variant TATA/-;TA;TATATA;TATATATA;TATATATATA;TATATATATATA delins 16