Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1800472 0.752 0.360 19 41341955 missense variant G/A snv 2.6E-02 2.3E-02 11
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs1800630 0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14 17
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 0.69 108
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs1800972 0.708 0.440 8 6877901 5 prime UTR variant C/G;T snv 0.79 16
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs1927907 0.790 0.320 9 117710486 intron variant C/T snv 0.18 7
rs1927911 0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs2066844 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 54
rs2069837 0.724 0.520 7 22728408 intron variant A/C;G snv 18
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2070874
IL4
0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 27
rs2149356 0.742 0.360 9 117711921 intron variant T/G snv 0.54 14
rs2155052 1.000 0.040 11 102724935 5 prime UTR variant C/G snv 0.92 1
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2237892 0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 16
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48