Source: GWASDB

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
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
rs674302
ABO
9 133271249 intron variant A/T snv 8
rs545971
ABO
9 133267960 intron variant T/A;C snv 8
rs12721046 19 44917997 intron variant G/A snv 0.11 8
rs129128 6 26125114 intron variant C/T snv 0.91 7
rs644234
ABO
9 133266804 intron variant G/T snv 7
rs643434
ABO
9 133266942 intron variant A/G;T snv 7
rs2126259 1.000 8 9327636 intron variant T/C snv 0.87 7
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs228129 22 37032558 upstream gene variant A/G snv 0.48 6
rs130624 22 37042611 regulatory region variant G/T snv 0.47 6
rs17342717 6 25821542 intron variant C/T snv 6.1E-02 6
rs2413450 22 37074184 intron variant T/C snv 0.61 6
rs6982636 8 125467073 intron variant G/A snv 0.43 6
rs35381288 8 37965106 non coding transcript exon variant C/G snv 7.4E-03 6
rs2980880 8 125468730 intron variant G/A snv 0.69 6
rs533617 2 21011100 missense variant T/C snv 3.1E-02 2.9E-02 6
rs8138057 22 37665537 intron variant G/A snv 3.0E-03 1.3E-02 6
rs17240378 16 67942790 intron variant G/C;T snv 4.0E-06 6
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs11571151 11 101127486 missense variant C/G;T snv 6
rs1874148
VCL
10 74114657 intron variant A/G snv 1.8E-02 6
rs33980385 19 40991388 missense variant A/G snv 6
rs34183407 2 73454052 missense variant C/T snv 2.1E-05 3.5E-05 6