Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs387907272 0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs144848 0.653 0.440 13 32332592 missense variant A/C snv 0.28 0.23 29
rs568408 0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16 29
rs2308321 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 29
rs20575 0.645 0.440 8 23201811 missense variant C/G snv 0.54 0.44 29
rs1346044
WRN
0.708 0.440 8 31167138 missense variant T/C snv 0.24 0.23 23
rs1805377 0.689 0.480 5 83353124 splice acceptor variant G/A snv 0.23 0.25 19
rs9808753 0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs1805329 0.732 0.400 9 107322047 missense variant C/T snv 0.20 0.16 15
rs2682818 0.742 0.320 12 80935757 non coding transcript exon variant A/C;T snv 0.83 14
rs172378 0.790 0.240 1 22638945 synonymous variant A/G snv 0.49 0.51 11