Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs10936599 0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 32
rs156697 0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 25
rs17855750 0.695 0.480 16 28503907 missense variant A/C;T snv 6.4E-02; 4.0E-06 21
rs2295080 0.695 0.320 1 11262571 upstream gene variant G/C;T snv 20
rs937475913 0.790 0.120 8 47936435 missense variant T/C snv 4.0E-06 7