Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79105258 12 111280427 intron variant C/A;T snv 23
rs198851 6 26104404 downstream gene variant T/A;C;G snv 15
rs4841132 8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs13331259 16 249924 intron variant A/G snv 3.0E-02 14
rs201518227 1.000 1 179917914 missense variant C/T snv 3.2E-05 5.6E-05 13
rs3123543 1 212617344 intron variant T/A;C snv 13
rs7296503 12 41306962 intron variant C/T snv 0.57 13
rs4837892 9 121826025 intron variant G/T snv 0.36 13
rs76792961 16 243594 intron variant C/T snv 7.3E-03 13
rs112505971 10 27068541 intron variant A/C;G snv 13
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs7776054 6 135097778 intron variant A/G snv 0.24 13
rs3840870 17 50184820 3 prime UTR variant -/CTTG delins 13
rs9917425 20 16755400 intron variant G/T snv 0.16 13
rs7310615 0.882 12 111427245 intron variant C/G snv 0.67 12
rs3811444 1 247876149 missense variant C/T snv 0.31 0.26 12
rs35188965 5 1104823 intron variant C/G;T snv 12
rs1744297 14 104102135 intron variant T/C snv 0.86 12
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs1567010427 0.882 14 102010824 missense variant G/A snv 11
rs2277339 12 56752285 missense variant T/G snv 0.12 0.14 10
rs17758695 18 63253621 intron variant C/T snv 2.1E-02 10
rs218265 4 54542832 intergenic variant T/C snv 0.21 10
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs612169
ABO
9 133268030 intron variant G/A snv 10