Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs12304647 0.807 0.160 12 53991163 intron variant A/C snv 0.26 6
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs11564475 0.882 0.080 3 41238542 intron variant A/G snv 3.7E-02 3
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1927911 0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs2494752 0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs3742330 0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 24
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs4135385 0.742 0.320 3 41237949 non coding transcript exon variant A/G snv 0.19 14
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs4711998 0.708 0.360 6 52185555 upstream gene variant A/G snv 0.64 16