Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1415259 0.925 0.080 1 162115519 intron variant C/T snv 0.54 2
rs7296288
DHH
0.851 0.080 12 49086185 upstream gene variant A/C snv 0.50 2
rs9825823 0.851 0.080 3 61096480 intron variant T/C snv 0.47 2
rs1082214
MIP
0.925 0.080 12 56452706 non coding transcript exon variant C/T snv 9.3E-02 1
rs1106634 0.851 0.080 8 20208538 intron variant G/A;C;T snv 0.18 1
rs11824092 0.925 0.080 11 13324747 intron variant T/C snv 0.62 1
rs120074175 0.827 0.080 12 72031544 missense variant G/A snv 1.2E-05 7.0E-06 1
rs139315125 0.851 0.080 1 7809900 missense variant A/G snv 5.6E-03 5.0E-03 1
rs1488864 0.851 0.080 11 6321099 intron variant T/G snv 0.80 1
rs1491850 0.925 0.080 11 27728178 intron variant T/C snv 0.37 1
rs2522833 0.827 0.080 7 82824392 missense variant A/C snv 0.45 0.34 1
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs33939927 0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 2
rs4523957
SMG6 ; SRR
0.790 0.120 17 2305605 intron variant G/T snv 0.54 2
rs528732638 0.851 0.120 18 26940224 intron variant A/-;AA;AAA;AAAA delins 2
rs10514299 0.827 0.120 5 88367793 intron variant C/T snv 0.21 1
rs11754661 0.851 0.120 6 150885942 intron variant G/A;T snv 1
rs12912233 0.851 0.120 15 60974897 intron variant C/T snv 0.38 1
rs1545843 0.827 0.120 12 84170289 intron variant G/A snv 0.52 1
rs2028122 0.851 0.120 15 60549076 intron variant A/G snv 0.51 1
rs2300478 0.851 0.120 2 66554321 intron variant T/G snv 0.21 1
rs34436714 0.851 0.120 19 53824059 missense variant C/A;T snv 0.22 1
rs1131691771 0.807 0.160 6 78958469 splice donor variant ACTT/- delins 18
rs7103411 0.752 0.160 11 27678578 intron variant C/T snv 0.82 3
rs1863918 0.882 0.160 5 179112381 3 prime UTR variant G/T snv 0.25 1