Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 213
rs5780218 0.882 0.080 1 204196482 5 prime UTR variant A/- delins 0.44 4
rs61764370 0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs735482 0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16
rs13423759 0.925 0.080 2 211381247 3 prime UTR variant A/C snv 6.8E-02 3
rs4946728 1.000 0.120 6 106142488 intron variant A/C snv 0.72 3
rs6983561 0.925 0.080 8 127094635 intron variant A/C snv 0.17 3
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 45
rs4671393 0.790 0.400 2 60493816 intron variant A/C;G snv 9
rs11788747 0.851 0.240 9 36105267 synonymous variant A/C;G snv 4.0E-06; 0.34 6
rs11016879 0.882 0.040 10 129691518 intron variant A/C;G snv 0.66 4
rs121913512
KIT
0.851 0.120 4 54728055 missense variant A/C;G snv 4
rs6510502 1.000 0.080 19 35647577 upstream gene variant A/C;G snv 2
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 484
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 21
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 16
rs629849 0.827 0.160 6 160073377 missense variant A/C;G;T snv 0.90 0.91 8
rs121918461 0.827 0.240 12 112450362 missense variant A/C;G;T snv 5
rs772893086 0.925 0.080 21 45176099 missense variant A/C;G;T snv 4.0E-06 4
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs6505162 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs121913366 0.763 0.400 7 140753345 missense variant A/C;T snv 7
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73