Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs4665972 2 27375230 intron variant T/C snv 0.69 9
rs12721046 19 44917997 intron variant G/A snv 0.11 8
rs545971
ABO
9 133267960 intron variant T/A;C snv 8
rs643434
ABO
9 133266942 intron variant A/G;T snv 8
rs674302
ABO
9 133271249 intron variant A/T snv 8
rs11508026 16 56965416 intron variant C/T snv 0.32 7
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs12679834
LPL
8 19962922 intron variant T/C snv 9.4E-02 7
rs174529 11 61776489 intron variant T/C snv 0.34 7
rs644234
ABO
9 133266804 intron variant G/T snv 7
rs7203984 16 56965346 intron variant A/C snv 0.31 7
rs7499892 16 56972678 intron variant C/G;T snv 7
rs1041968 2 21009932 synonymous variant G/A snv 0.39 0.38 6
rs11207997 1 62596235 intron variant C/T snv 0.39 6
rs1167998 1 62465961 intron variant C/A snv 0.57 6
rs12720922 16 56966973 intron variant G/A snv 0.23 6
rs2131925 1 62560271 intron variant G/T snv 0.57 6
rs217181 16 72080103 intron variant C/T snv 0.20 6
rs2731672 5 177415473 intron variant T/C snv 0.66 6
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 6
rs583104 1 109278685 downstream gene variant G/T snv 0.63 6
rs6065906 20 45925376 downstream gene variant T/A;C;G snv 6
rs660240 1 109275216 3 prime UTR variant T/C snv 0.75 6
rs7200543 16 15036113 synonymous variant A/G snv 0.35 0.30 6