Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs1011970 0.677 0.320 9 22062135 intron variant G/T snv 0.23 22
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs11119608 0.708 0.280 1 210816167 intron variant T/G snv 0.21 17
rs11168936 0.708 0.280 12 49251457 intron variant T/A;C snv 17
rs11200014 0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 19
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs115392158 0.708 0.280 6 31347004 intron variant A/G snv 17
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs11844632 0.708 0.280 14 68559662 intron variant G/A snv 0.23 17
rs11907546 0.708 0.280 20 34131991 upstream gene variant C/A;T snv 17
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs12601991 0.708 0.280 17 37741642 intron variant T/A;G snv 17
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs12976445 0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45 20
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs147527678 0.708 0.280 6 32699696 intergenic variant G/A;C snv 17
rs147680653 0.708 0.280 6 29785031 intergenic variant A/G snv 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1571801 0.827 0.120 9 121665094 intron variant G/T snv 0.21 6