Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11152369 0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 5
rs1176744 0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs17673138 0.851 0.040 8 32840440 intron variant A/C snv 8.6E-02 4
rs7296288
DHH
0.851 0.080 12 49086185 upstream gene variant A/C snv 0.50 5
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs878567 0.882 0.040 5 63960164 intron variant A/C;G snv 4
rs12487445 0.925 0.040 3 52584303 intron variant A/C;T snv 2
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs1042779 0.882 0.040 3 52786995 missense variant A/G snv 0.40 0.42 4
rs10748045 0.925 0.040 12 66422359 intron variant A/G snv 0.41 3
rs10968749 0.851 0.040 9 28752486 intergenic variant A/G snv 5.5E-02 4
rs11191454 0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 9
rs11773103 0.925 0.040 7 87192664 non coding transcript exon variant A/G snv 4.5E-02 2
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12576775 0.827 0.080 11 79366149 intron variant A/G snv 0.15 6
rs140504 0.882 0.040 22 23285182 missense variant A/G snv 0.81 0.86 3
rs16836940 0.925 0.040 1 150444437 intron variant A/G snv 0.31 2
rs17082664 0.925 0.040 6 152417619 intron variant A/G snv 0.17 2
rs17158930 0.851 0.040 7 111871082 intron variant A/G snv 0.25 4
rs17387100 0.925 0.040 4 15993502 intron variant A/G snv 7.5E-02 3
rs17662626 0.851 0.040 2 193119895 intergenic variant A/G snv 5.9E-02 5
rs1801260 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135