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
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 8
rs545971
ABO
9 133267960 intron variant T/A;C snv 8
rs674302
ABO
9 133271249 intron variant A/T snv 8
rs643434
ABO
9 133266942 intron variant A/G;T snv 7
rs644234
ABO
9 133266804 intron variant G/T snv 7
rs11508026
CETP
16 56965416 intron variant C/T snv 0.32 5
rs1169313
C12orf43
12 121004867 intron variant T/A;C snv 4
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 4
rs3758348
SURF4
9 133372523 intron variant G/C snv 0.13 4
rs6065906 20 45925376 downstream gene variant T/A;C;G snv 4
rs7518199
IL6R
1 154434943 intron variant A/C;T snv 0.39; 4.2E-06 4
rs10512597
RAB37 ; CD300LF
17 74703694 intron variant T/A;C snv 3
rs12967135 18 60181790 intergenic variant G/A snv 0.24 3
rs3027012
CADM3-AS1 ; ACKR1
1 159204333 5 prime UTR variant C/T snv 0.13 3
rs10761731
JMJD1C
10 63267850 intron variant A/T snv 0.38 2
rs10891343
BCO2
11 112209661 intron variant T/C snv 0.44 2
rs10908713 1 159369769 intron variant T/C snv 0.47 2
rs11265174 1 159350569 intron variant T/A snv 0.35 2
rs11265190
OR10J1
1 159421611 intron variant G/A snv 0.47 2
rs11265196 1 159448422 intron variant G/A snv 0.47 2
rs1169310
C12orf43 ; HNF1A
12 121001630 3 prime UTR variant G/A snv 0.31 2
rs12034383
CR1
1 207630250 intron variant G/A snv 0.47 2
rs12034864 1 159215190 regulatory region variant A/C;G;T snv 2