Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs729302 0.827 0.160 7 128928906 intergenic variant A/C snv 0.28 6
rs17465637 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
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
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1057523354 0.763 0.480 13 110179387 missense variant C/A snv 13
rs2779249 0.851 0.200 17 27801555 intron variant C/A snv 0.33 7
rs549591993
F7
0.776 0.400 13 113105794 5 prime UTR variant C/A snv 4.0E-04 2.8E-05 12
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs2305948
KDR
0.732 0.400 4 55113391 missense variant C/A;T snv 4.0E-06; 0.11 18
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193