Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799732 0.790 0.160 11 113475529 intron variant -/G delins 11
rs627928 0.790 0.080 1 182582202 missense variant A/C snv 0.54 0.49 10
rs63750416 0.851 0.120 17 46010373 missense variant A/C snv 7
rs28933088 0.925 0.080 17 41624218 missense variant A/C snv 2
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs63750231 0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs767543900 0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 10
rs80357033 0.925 0.200 17 43106467 missense variant A/C;G snv 2
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs879254382 0.882 0.080 19 11089549 start lost A/C;G;T snv 3
rs80265967 0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03 16
rs2682818 0.742 0.320 12 80935757 non coding transcript exon variant A/C;T snv 0.83 14
rs993022333
KIT
0.851 0.080 4 54733173 missense variant A/C;T snv 5
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs3803662 0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs876658657 0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs2981582 0.695 0.360 10 121592803 intron variant A/G snv 0.58 21
rs13387042 0.732 0.280 2 217041109 intergenic variant A/G snv 0.44 16
rs10993994 0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54 15
rs121918075
TTR
0.752 0.280 18 31598632 missense variant A/G snv 15
rs17125721 0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14