Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10052657 0.807 0.120 5 59111944 intron variant C/A snv 0.17 7
rs10061133 0.851 0.160 5 55170716 mature miRNA variant A/G snv 0.11 8.6E-02 4
rs1009316
BAX
1.000 0.080 19 48955313 non coding transcript exon variant T/C;G snv 1
rs10138277 1.000 0.080 14 31393927 intron variant T/A;C snv 1
rs10204525 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 20
rs1029342144 0.882 0.120 10 87864162 5 prime UTR variant C/G;T snv 6
rs1033667 1.000 0.080 22 28734312 intron variant C/T snv 0.30 1
rs1035142 0.807 0.200 2 201288355 3 prime UTR variant T/C;G snv 0.54 7
rs1042026 1.000 0.080 4 99307309 3 prime UTR variant T/C snv 0.24 2
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs10484761 0.807 0.080 6 40834522 intergenic variant T/C snv 0.31 7
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1050631 0.882 0.080 18 36114157 synonymous variant G/A snv 0.33 0.30 4
rs10511729 0.742 0.240 9 23557229 intron variant T/G snv 0.35 11
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1063192 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 24
rs107822 0.827 0.120 6 33207798 upstream gene variant C/T snv 0.27 0.28 5
rs10811474 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 11
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs10882379 1.000 0.080 10 93991742 intergenic variant G/A;C snv 1
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27