Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6586354 0.851 0.040 1 234897489 intron variant G/A snv 0.25 4
rs111365677 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-03 3
rs4839421 0.925 0.040 1 110479338 intron variant C/A snv 0.40 3
rs55679149 0.925 0.040 1 89068655 upstream gene variant C/T snv 0.34 3
rs7555693 0.925 0.040 1 106295917 intergenic variant G/A snv 0.45 3
rs782212 0.925 0.040 1 72479983 intron variant C/T snv 0.34 2
rs2984618 0.925 0.040 1 47224766 intron variant G/T snv 0.52 1
rs760161369 0.882 0.040 1 11800214 missense variant G/A;C snv 2.8E-05; 4.0E-06 1
rs2302045 0.851 0.040 2 241081801 splice region variant G/A snv 7.6E-02 1.0E-01 4
rs6546604 0.925 0.040 2 70415675 intron variant G/A;T snv 3
rs78087832 0.925 0.040 2 224600060 intergenic variant C/T snv 2.4E-03 3
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 1
rs6740584 0.882 0.040 2 207564627 intron variant T/C snv 0.37 1
rs9862857 0.851 0.040 3 30453840 regulatory region variant A/G;T snv 4
rs11924809 0.925 0.040 3 186353656 intron variant G/A snv 5.3E-02 3
rs139459337 0.882 0.040 3 114997018 intron variant C/T snv 4.7E-02 3
rs142484554 0.925 0.040 3 141059454 intron variant GAG/- delins 0.11 3
rs4685959 0.925 0.040 3 5645577 regulatory region variant C/G;T snv 2
rs76767803 0.925 0.040 3 36230378 intergenic variant C/T snv 0.16 2
rs9825823 0.851 0.080 3 61096480 intron variant T/C snv 0.47 2
rs112538845 0.925 0.040 4 184084475 downstream gene variant C/T snv 1.7E-02 3
rs11728985 0.925 0.040 4 129115280 3 prime UTR variant C/T snv 0.12 3
rs189864513 0.925 0.040 4 52767390 intron variant T/C snv 1.9E-03 3
rs1908557 0.925 0.040 4 89500202 intron variant T/C snv 0.31 3
rs34177316 0.925 0.040 4 40985283 intron variant A/-;AA;AAA delins 3