Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11554137 0.742 0.040 2 208248468 synonymous variant G/A snv 5.1E-02 6.8E-02 13
rs753152604 0.827 0.040 12 57751680 missense variant C/A snv 7
rs1373481065 0.827 0.040 1 67687668 missense variant A/G snv 4.0E-06 6
rs1005230 0.827 0.040 6 43768759 upstream gene variant T/C snv 0.60 5
rs11860248 0.882 0.040 16 24566445 intron variant T/G snv 0.27 5
rs11979158 0.882 0.040 7 55091656 intron variant A/G;T snv 0.20 5
rs1385943435 0.851 0.040 9 37002662 missense variant C/A;G;T snv 4.1E-06; 4.1E-06 5
rs1920116 0.882 0.040 3 169862183 intron variant G/A snv 0.25 5
rs2234248 0.827 0.040 6 41163980 upstream gene variant A/G snv 2.2E-03 5
rs2252586 0.882 0.040 7 54911231 intergenic variant C/T snv 0.27 5
rs3092993 0.827 0.040 11 108364388 intron variant C/A snv 0.11 5
rs374052197 0.882 0.040 1 13610421 missense variant G/A;T snv 8.0E-06 5
rs374524467 0.827 0.040 4 110632961 missense variant A/C snv 8.0E-06 7.0E-06 5
rs71305152 0.882 0.040 8 105437494 intron variant -/TTTTCT delins 0.43 5
rs745934102 0.882 0.040 1 13607281 missense variant G/A snv 3.2E-05 1.4E-05 5
rs760031382 0.851 0.040 9 36966613 missense variant C/T snv 8.0E-06 5
rs865880036 0.827 0.040 15 37098156 missense variant A/C snv 1.3E-04 5
rs10852606 0.882 0.040 16 50094961 intron variant T/A;C snv 4
rs11079041 0.882 0.040 17 42262061 intron variant T/A;C snv 0.36 4
rs11233250 0.882 0.040 11 82685972 intron variant C/T snv 0.11 4
rs12230172 0.882 0.040 12 75848895 intron variant A/G snv 0.48 4
rs12752552 0.882 0.040 1 64763616 intron variant T/C snv 0.13 4
rs1801591 0.882 0.040 15 76286421 missense variant G/A snv 7.4E-02 6.4E-02 4
rs2235573 0.882 0.040 22 38081923 synonymous variant G/A snv 0.47 0.46 4
rs2562152 0.882 0.040 16 73898 intron variant A/T snv 0.67 4