Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1169089134 0.790 0.320 11 49206785 missense variant C/G;T snv 9
rs1206846668 0.724 0.400 11 49185773 missense variant G/A snv 4.1E-06 16
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12413409 0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 9
rs1279844744 0.925 0.080 15 74720521 missense variant A/G snv 3
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs1368310331 0.827 0.200 15 74723032 synonymous variant T/C snv 7.0E-06 6
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
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
rs1979277 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 45
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82