Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519999 0.763 0.160 17 7674247 missense variant T/C;G snv 12
rs1057520003 0.695 0.320 17 7675996 missense variant T/G snv 20
rs1057520007 0.701 0.440 17 7674917 missense variant T/A;C;G snv 21
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11554273 0.689 0.240 20 58909365 missense variant C/A;G;T snv 4.0E-06 22
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53
rs121912655 0.724 0.400 17 7674238 missense variant C/A;G;T snv 15
rs121912656 0.662 0.560 17 7674229 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 28
rs121912660 0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 34
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 37
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 26
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs121913385 0.763 0.240 9 21971112 missense variant G/A;C snv 9
rs121913399 0.724 0.200 3 41224612 missense variant G/A;C snv 13