Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10224002 0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs11097432 1.000 0.080 4 94658554 intron variant T/C snv 0.24 2
rs1150256 0.925 0.120 1 206899788 intron variant G/A snv 0.40 4
rs12413409 0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 9
rs12500426 0.851 0.240 4 94593458 intron variant A/C snv 0.54 5
rs12576239 1.000 0.080 11 2481089 intron variant C/T snv 0.16 3
rs13306519 1.000 0.080 1 65572246 intron variant C/G;T snv 2
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs13333226 0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs146052672 0.851 0.160 6 34242693 intron variant -/C delins 5
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs1572982
HFE
0.827 0.200 6 26094139 intron variant G/A;T snv 0.52; 8.0E-06 7
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1993116 0.827 0.200 11 14888688 intron variant A/G snv 0.65 8
rs2070895 0.807 0.120 15 58431740 intron variant G/A snv 0.33 15
rs223331 0.851 0.160 4 102872408 intron variant T/A;C snv 5
rs2237892 0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 16
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 17