Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12478841
ZNF512
0.925 0.120 2 27588855 intron variant A/G snv 0.27 5
rs2384656
ZNF512
0.925 0.120 2 27609188 intron variant A/G snv 0.27 5
rs4666000
ZNF512
0.925 0.120 2 27616502 intron variant T/C snv 0.28 5
rs6760250
ZNF512
0.925 0.120 2 27589385 intron variant G/A;C snv 5
rs2420371
F5
1 169522317 intron variant G/A snv 0.95 4
rs13030973
LINC01460
0.925 0.120 2 27705930 non coding transcript exon variant T/C snv 0.17 4
rs4616435
LINC01460
0.925 0.120 2 27710775 intron variant C/T snv 0.17 4
rs6727215
LINC01460
0.925 0.120 2 27711864 intron variant G/A snv 0.17 4
rs6727388
LINC01460
0.925 0.120 2 27709720 intron variant A/G;T snv 4
rs13023094
SLC4A1AP
0.925 0.120 2 27687839 intron variant A/C snv 0.16 4
rs2272406
SLC4A1AP
0.925 0.120 2 27669156 intron variant A/T snv 0.17 4
rs7777102 7 73643687 intergenic variant A/G;T snv 3
rs2295888
EDEM2 ; MMP24-AS1-EDEM2
20 35135060 intron variant A/G snv 0.14 3
rs2065108
MMP24-AS1-EDEM2 ; EDEM2
1.000 0.080 20 35119019 intron variant C/T snv 0.61 3
rs6088727
MMP24-AS1-EDEM2 ; EDEM2
1.000 0.080 20 35125836 intron variant G/A snv 0.51 3
rs6060038
NCOA6
1.000 0.080 20 34769912 intron variant G/A snv 0.45 3
rs6141509
NCOA6
1.000 0.080 20 34731584 intron variant G/A snv 0.45 3
rs1158867
PROC
1.000 0.080 2 127419801 splice region variant C/T snv 0.51 3
rs1885119
TRPC4AP
1.000 0.080 20 35057846 intron variant T/C snv 0.58 3
rs3736802
TRPC4AP
1.000 0.080 20 35016239 intron variant T/C snv 0.53 3
rs3818253
TRPC4AP
1.000 0.040 20 35009073 intron variant G/A snv 0.19 3
rs6087664
TRPC4AP
1.000 0.080 20 35038413 intron variant C/A;G;T snv 3
rs6088692
TRPC4AP
1.000 0.080 20 35050785 intron variant A/G snv 0.58 3
rs6120816
TRPC4AP
1.000 0.080 20 35056555 intron variant G/A;C snv 3
rs1040552 20 33861523 regulatory region variant A/G snv 0.19 2