Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs800437 1.000 0.080 4 24788541 upstream gene variant A/G snv 0.97 1
rs1879997
NR1I2
3 119802381 intron variant T/C snv 0.97 2
rs6431731
LINC01804
1.000 0.080 2 15722878 intron variant C/T snv 0.97 1
rs807773
LINC01182 ; LOC107986182
1.000 0.080 4 13897376 intron variant T/A snv 0.97 1
rs11784828
MSRA
8 10333788 intron variant T/G snv 0.97 1
rs10954843
NRG1
8 32419595 intron variant G/A snv 0.97 2
rs4772643
LOC107984607 ; LOC107984606
1.000 0.080 13 104829705 intergenic variant G/A snv 0.97 1
rs9684265
CLNK
4 10588037 intron variant G/A snv 0.97 1
rs804532 1.000 0.080 20 22148917 intergenic variant G/A snv 0.97 1
rs4789937
CEP295NL ; TIMP2
17 78898598 non coding transcript exon variant A/G snv 0.97 1
rs804527 1.000 0.080 20 22143779 intergenic variant G/T snv 0.97 1
rs804529 1.000 0.080 20 22145246 regulatory region variant A/C snv 0.97 1
rs804530 1.000 0.080 20 22147832 intergenic variant T/C snv 0.97 1
rs708997 1.000 0.080 20 22146410 intergenic variant A/C snv 0.97 1
rs6561821
STARD13
13 33287048 intron variant A/T snv 0.97 1
rs708999 1.000 0.080 20 22147256 intergenic variant C/T snv 0.97 1
rs804538 1.000 0.080 20 22155635 intergenic variant G/A snv 0.97 1
rs804536 1.000 0.080 20 22154669 intergenic variant T/C snv 0.97 1
rs1365771
LIPC
15 58568503 intron variant T/A snv 0.96 2
rs2206754 1.000 0.080 20 22125205 intergenic variant T/C snv 0.96 1
rs2820301
LMOD1
1 201943694 intron variant G/A snv 0.96 2
rs6047915 1.000 0.080 20 22121515 intergenic variant T/C snv 0.96 1
rs201142 1.000 0.080 20 22106222 regulatory region variant G/A snv 0.96 1
rs201144 1.000 0.080 20 22106900 regulatory region variant A/G snv 0.96 1
rs1586840 1.000 0.080 12 19909563 intron variant G/A snv 0.96 1