Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs1800471 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 33