Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs174533 0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 18
rs174583 0.807 0.320 11 61842278 intron variant C/T snv 0.35 16
rs2232365 0.716 0.480 X 49259429 intron variant T/C snv 16
rs174576 0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs174594 0.776 0.160 11 61852357 intron variant C/A;T snv 14
rs603424 1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs7708392 0.732 0.400 5 151077924 intron variant G/C snv 0.44 13
rs10887800 0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs13333226 0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs2236242 0.776 0.280 14 94493715 intron variant T/A snv 0.31 9
rs4821480 0.807 0.160 22 36299201 intron variant G/T snv 0.78 9
rs17173608 0.807 0.240 7 150339575 intron variant T/G snv 0.11 8
rs174541 1.000 0.080 11 61798436 intron variant T/C snv 0.29 8
rs174566 0.925 0.160 11 61824890 intron variant A/G snv 0.34 8
rs2294021 0.776 0.280 X 49249149 intron variant T/A;C snv 0.52 8
rs4293393 0.827 0.200 16 20353266 intron variant A/G snv 0.20 8
rs11622435 0.827 0.120 14 81151652 intron variant G/A snv 4.7E-02 7