Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1012477 0.827 0.160 1 7798075 intron variant G/C snv 0.16 8
rs10165970 0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs10519097 0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs11943456 0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs17024869 0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs2298881 0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs28360071 0.708 0.240 5 83142293 intron variant GATGAGGAAACTAACTCTCAGTGGTGTTTA/- delins 0.48 18
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs5743551 0.742 0.240 4 38806033 intron variant T/A;C snv 12
rs6869366 0.701 0.280 5 83075927 intron variant T/G snv 9.2E-02 18
rs7581886 0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs895520 0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs9651118 0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs10012 0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 16
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77