Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs3480 0.807 0.160 1 32862564 3 prime UTR variant G/A snv 0.56 8
rs797044485 0.851 0.160 1 156134832 missense variant G/A snv 4
rs12137855 0.882 0.040 1 219275036 downstream gene variant C/T snv 0.19 3
rs12743824 0.925 0.040 1 99317401 intergenic variant C/A snv 0.48 2
rs772114791 1.000 0.040 1 55052343 missense variant G/A snv 8.0E-06 7.0E-06 1
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs886041065 0.677 0.600 2 25743913 frameshift variant G/- delins 43
rs1553403917 0.807 0.320 2 73451171 frameshift variant -/A delins 7
rs17007417 0.882 0.080 2 71808541 regulatory region variant T/C snv 0.85 3
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs951599607 0.925 0.040 3 12434028 missense variant G/A snv 4
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs72613567 0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs10833 0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 10
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs1057972 0.790 0.200 4 141733279 3 prime UTR variant A/T snv 0.54 7
rs2290602 0.882 0.040 4 23824109 intron variant T/A;G snv 3