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
rs144848 0.653 0.440 13 32332592 missense variant A/C snv 0.28 0.23 29
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1799977 0.662 0.440 3 37012077 missense variant A/C;G;T snv 0.23 28
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
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
rs3803662 0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs851797 0.752 0.240 1 241889740 3 prime UTR variant A/G snv 0.72 13
rs876658657 0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs17561 0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26 23
rs1899663 0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33