Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12576775 0.827 0.080 11 79366149 intron variant A/G snv 0.15 6
rs3812036 0.925 0.120 5 177386403 intron variant C/T snv 0.23 0.20 5
rs1481017 0.882 0.160 4 88176325 intron variant C/T snv 0.59 4
rs2622629 0.882 0.160 4 88172912 intron variant T/C snv 0.28 4
rs4971059 0.851 0.200 1 155176305 intron variant G/A snv 0.34 4
rs652722 1.000 0.040 11 31883988 intron variant C/T snv 0.32 4
rs10054105 0.925 0.080 5 111573636 intron variant T/G snv 0.17 3
rs10821871 0.882 0.160 10 50824350 intron variant T/C snv 0.22 3
rs10994720 0.882 0.160 10 50852341 intron variant G/A snv 0.21 3
rs11709077 0.925 0.120 3 12295008 intron variant G/A snv 8.8E-02 3
rs11815391 0.882 0.160 10 50818978 intron variant A/G snv 0.26 3
rs11978267 0.763 0.240 7 50398606 intron variant A/G snv 0.25 3
rs12133576
DR1
1.000 0.040 1 93350843 intron variant A/G snv 0.51 3
rs12199222 1.000 0.040 6 17699091 intron variant G/A;T snv 3
rs1353747 0.882 0.080 5 59041654 intron variant T/G snv 6.9E-02 3
rs1481014 0.882 0.160 4 88175999 intron variant C/A;T snv 0.24 3
rs17036328 1.000 0.040 3 12348985 intron variant T/C snv 0.14 3
rs17056278 0.925 0.040 5 158825430 intron variant C/G snv 5.3E-02 3
rs17806888 1.000 0.040 3 67365898 intron variant T/C snv 9.1E-02 3
rs2127863 0.882 0.160 4 88190316 intron variant T/C snv 0.84 3
rs2622590 0.925 0.080 8 55445714 intron variant G/A snv 0.15 3
rs36600 0.827 0.080 22 29941597 intron variant T/C snv 0.78 3
rs41520844
WRN
0.882 0.080 8 31135670 intron variant A/T snv 7.1E-02 3
rs4327572 0.882 0.120 5 25972712 intron variant C/T snv 0.28 3
rs4364959 0.882 0.080 10 21996442 intron variant C/T snv 0.77 3