Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587777308 0.763 0.040 5 161873196 missense variant G/A snv 14
rs587777057 0.827 0.040 16 56336744 missense variant G/A snv 8
rs10868235 0.925 0.040 9 84878840 intron variant C/T snv 0.40 6
rs145999922 0.882 0.040 2 227699378 missense variant A/G snv 4.4E-05 4.2E-05 5
rs121918803 0.851 0.040 2 166009745 missense variant C/G snv 4
rs796052493 0.851 0.040 5 161895668 missense variant G/A;T snv 4
rs869320632 0.925 0.040 2 96739883 missense variant C/T snv 4
rs1057518988 0.925 0.040 12 13571859 missense variant T/C snv 3
rs121912707 0.925 0.040 5 126552059 missense variant C/G snv 3.6E-04 2.4E-04 3
rs121917986 0.882 0.040 2 166002588 missense variant C/G;T snv 3
rs121918612 0.925 0.040 1 160127704 missense variant G/A snv 3
rs1553709380 0.925 0.040 3 113778833 missense variant C/G snv 3
rs192669225 0.925 0.040 1 109628692 missense variant G/A snv 3
rs200345816 0.925 0.040 7 102283048 missense variant C/G;T snv 6.0E-05; 4.0E-06 3
rs2298771 0.925 0.040 2 166036278 missense variant C/T snv 0.73 0.74 3
rs372292910 1.000 0.040 5 141122905 frameshift variant A/-;AA delins 1.7E-04 3
rs387906683 0.882 0.040 2 165297053 stop gained C/T snv 3
rs587777459 0.882 0.040 22 31815005 stop gained C/G;T snv 2.0E-05 3
rs6755571 1.000 0.040 2 233718890 missense variant C/A;T snv 3.6E-02; 4.0E-06 3
rs730882200 0.882 0.040 20 48953604 frameshift variant -/C delins 3
rs730882222 0.925 0.040 17 6707026 splice donor variant A/C snv 3
rs730882229 0.882 0.040 3 47411889 missense variant G/A;T snv 8.0E-06 3
rs74315322 1.000 0.040 1 154275165 stop gained C/T snv 3.6E-05 3
rs765078446 0.925 0.040 6 53013900 missense variant T/G snv 2.0E-05 2.1E-05 3
rs886044717 0.925 0.040 9 135779423 missense variant T/A snv 3