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
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
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs17251221 0.724 0.360 3 122274400 intron variant A/G snv 0.11 18
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
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
rs1993116 0.827 0.200 11 14888688 intron variant A/G snv 0.65 8
rs20551 0.752 0.320 22 41152004 missense variant A/G snv 0.31 0.23 10
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13 11
rs3741219 0.776 0.280 11 1995389 non coding transcript exon variant A/G snv 0.42 10
rs3742330 0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 24
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4969168 0.790 0.480 17 78357712 3 prime UTR variant A/G snv 0.71 7