Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1337916669 0.925 0.040 6 26092879 missense variant G/T snv 2
rs1429117513 0.925 0.040 12 6775316 synonymous variant T/C snv 4.0E-06 2
rs1595064 0.925 0.040 2 211378020 3 prime UTR variant G/A;C snv 2
rs1595065 0.925 0.040 2 211377916 3 prime UTR variant G/A snv 0.73 2
rs17859821 1.000 0.040 16 55478141 intron variant G/A;C snv 0.11 2
rs1805126 0.925 0.040 3 38550915 synonymous variant A/G snv 0.39 0.44 2
rs2241562 0.925 0.040 5 175684809 intron variant G/C;T snv 1.0E-03 2
rs3212247 0.925 0.040 14 24340589 upstream gene variant A/G snv 0.12 2
rs3212254 0.925 0.040 14 24336257 missense variant G/A;T snv 1.2E-05; 7.3E-02 2
rs34376731 0.925 0.040 12 54581014 missense variant C/T snv 4.6E-03 1.9E-02 2
rs3748960 0.925 0.040 2 211383109 3 prime UTR variant C/T snv 0.96 2
rs452159
ADA
1.000 0.040 20 44642461 intron variant G/T snv 0.28 2
rs6123837 0.925 0.040 20 58890516 synonymous variant G/A snv 0.30 2
rs6684209 1.000 0.040 1 115707991 intron variant C/T snv 0.17 2
rs6787362 0.925 0.040 3 69178228 intron variant A/G snv 9.3E-02 2
rs7521023 1.000 0.040 1 115700759 3 prime UTR variant G/A snv 0.64 2
rs762151808 0.925 0.040 14 94378559 missense variant A/C snv 4.0E-06 7.0E-06 2
rs772608361 1.000 0.040 6 26087503 missense variant G/A;C snv 4.0E-06; 8.0E-06 2
rs9303504 0.925 0.040 17 66319248 intron variant G/C snv 0.59 2
rs9885413 0.925 0.040 5 110840429 intergenic variant G/T snv 0.19 2
rs9909004 0.925 0.040 17 66310015 intron variant C/T snv 0.59 2
rs1009388 1.000 0.040 2 25168232 intron variant G/C snv 0.18 1
rs1544223 1.000 0.040 1 111503935 intron variant C/T snv 0.72 1
rs200432861 1.000 0.040 6 51775844 missense variant G/A;C snv 2.4E-05; 2.0E-05 1
rs3754860 1.000 0.040 2 25170385 upstream gene variant C/T snv 0.22 1