Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1048638
CA9
0.807 0.160 9 35681125 3 prime UTR variant C/A;G snv 10
rs735482 0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16
rs187115 0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs1801270 0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05 22
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs765660823 0.882 0.200 1 162778720 missense variant A/C snv 1.9E-04 4
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs751402 0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs1047840 0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77