Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2057482 0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs10009228 4 40354405 missense variant A/G snv 0.78 0.76 1
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 23
rs11672691 0.925 0.080 19 41479679 non coding transcript exon variant G/A snv 0.42 3
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1042028 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs720012 22 20111059 3 prime UTR variant G/A snv 0.12 1
rs2073778 22 20087052 non coding transcript exon variant C/T snv 0.12 1
rs55958994 0.925 0.080 12 52907235 intron variant C/T snv 0.12 3
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs3136797 0.827 0.120 8 42369287 missense variant C/G snv 1.1E-02 1.1E-02 10
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs367597251 0.807 0.080 12 68839587 missense variant A/G snv 1.5E-04 5.1E-04 10
rs200863613 0.925 0.080 9 21971061 missense variant C/A;T snv 8.5E-05 3.7E-04 6
rs121917887 0.790 0.120 17 51161744 missense variant A/G snv 6.0E-05 7.0E-05 10
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs969139366 4 54277974 missense variant T/C snv 3.5E-05 3
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs1443465532 0.882 0.080 6 43774362 missense variant G/C snv 4.0E-06 7.0E-06 6