Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 35
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 107
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 118
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 169
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs1859168 0.790 0.160 7 27202740 non coding transcript exon variant A/C;G;T snv 9
rs2031920 0.695 0.240 10 133526341 non coding transcript exon variant C/T snv 3.1E-02 20
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 75
rs2072454 0.763 0.160 7 55146655 synonymous variant C/T snv 0.51 0.51 9
rs213210 0.742 0.240 6 33208047 upstream gene variant A/C;G snv 10
rs217727 0.641 0.480 11 1995678 non coding transcript exon variant G/A snv 0.20 32
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 98
rs2240688 0.790 0.160 4 15968726 3 prime UTR variant T/G snv 0.22 7
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 36
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 37
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 39