Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs752742313 0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs2066827 0.695 0.320 12 12718165 missense variant T/A;C;G snv 1.6E-04; 1.6E-05; 0.26 21
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 32
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs20576 0.637 0.400 8 23200707 missense variant T/G snv 0.15 0.14 34
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs2424913 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 18
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205