Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs17293632 0.763 0.240 15 67150258 intron variant C/T snv 0.17 12
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1847472 0.807 0.200 6 90263440 intron variant C/A snv 0.25 7
rs1861494 0.716 0.400 12 68157629 intron variant C/T snv 0.75 15
rs1893217 0.742 0.440 18 12809341 intron variant A/G snv 0.12 14
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs2188962 0.882 0.160 5 132435113 intron variant C/T snv 0.29 5
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs4696480 0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs4845604 0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs5743836 0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs744166 0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs8005161 0.882 0.120 14 88006251 intron variant C/T snv 0.18 5
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 12
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 12
rs7746082 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 5
rs61816761 0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs16969968 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46