Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs895520 0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs2298881 0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs768623239 0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs1800440 0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 29
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs4646903 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 36
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55