Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs25487 0.485 0.679 19 43551574 missense variant T/C snp 0.68 0.72 119
rs11540654 0.492 0.679 17 7676040 missense variant C/A,G,T snp 4.8E-05 3.2E-05 117
rs1045642 0.520 0.714 7 87509329 synonymous variant A/G,T snp 0.50 0.56 108
rs1799782 0.523 0.607 19 43553422 stop gained G/A snp 9.5E-02 7.1E-02 84
rs13181 0.525 0.536 19 45351661 stop gained T/A,G snp 4.0E-06; 0.32 0.32 82
rs1052133 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 77
rs1805087
MTR
0.538 0.679 1 236885200 missense variant A/G snp 0.20 0.21 75
rs671 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 61
rs1799793 0.585 0.500 19 45364001 missense variant C/A,T snp 7.1E-06; 0.29 0.27 51
rs1229984 0.622 0.393 4 99318162 missense variant T/C,G snp 0.90 0.94 50
rs1801131 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 49
rs25489 0.587 0.571 19 43552260 stop lost C/G,T snp 8.5E-06; 7.1E-02 3.2E-05; 5.5E-02 48
rs1130409 0.590 0.500 14 20456995 missense variant T/A,C,G snp 4.0E-06; 4.0E-06; 0.42 0.44 45
rs104894230 0.615 0.464 11 534288 missense variant C/A,G,T snp 42
rs1800566 0.605 0.571 16 69711242 missense variant G/A snp 0.25 0.21 41
rs1801155
APC
0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 31
rs532358159 0.634 0.536 16 69711143 missense variant G/A snp 4.0E-06 30
rs1051740 0.647 0.429 1 225831932 missense variant T/C snp 0.32 0.28 29
rs2234922 0.652 0.321 1 225838705 missense variant A/G,T snp 0.19; 2.8E-05 0.23 28
rs758272654 0.667 0.536 20 58909201 synonymous variant T/C snp 4.0E-06 28
rs1051266 0.647 0.500 21 45537880 missense variant T/C,G snp 0.55; 4.4E-06 0.51 28
rs3212227 0.647 0.536 5 159315942 3 prime UTR variant T/G snp 0.25 27
rs28934578 0.647 0.357 17 7675088 missense variant snp 4.0E-06 27
rs4938723 0.657 0.357 11 111511840 intron variant T/C snp 0.33 26
rs11615 0.667 0.286 19 45420395 synonymous variant A/G snp 0.50 0.54 23