Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11209002
C1orf141
1.000 0.040 1 67124778 intron variant T/C snv 0.77 1
rs3810936
TNFSF15
0.742 0.320 9 114790605 synonymous variant T/C snv 0.71 0.75 1
rs2451258
LOC112267968
0.807 0.160 6 159085568 intron variant C/T snv 0.75 2
rs4263839
TNFSF15
0.807 0.160 9 114804160 intron variant A/G snv 0.75 3
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 2
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 1
rs17119
LOC101928354
0.882 0.120 6 14719265 intron variant G/A snv 0.74 1
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73 3
rs272888
MIR3936HG ; SLC22A4
1.000 0.040 5 132329730 intron variant T/C snv 0.71 1
rs582757
TNFAIP3
0.776 0.320 6 137876687 intron variant C/T snv 0.70 1
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 1
rs2248116
IRF1-AS1
1.000 0.040 5 132468655 intron variant C/A snv 0.70 1
rs2315008
ZGPAT
0.925 0.120 20 63712604 intron variant T/G snv 0.70 2
rs1109863 1.000 0.040 16 50658453 intergenic variant G/A snv 0.69 1
rs1456893 0.851 0.160 7 50230076 intron variant G/A snv 0.69 3
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 1
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69 1
rs8057341
NOD2
0.925 0.080 16 50704069 intron variant A/G snv 0.68 1
rs3094188
POU5F1 ; PSORS1C3
0.882 0.200 6 31174468 intron variant C/A;T snv 0.68 1
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs6863411
NDFIP1
0.827 0.120 5 142133639 intron variant A/T snv 0.67 1
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs9297145
KPNA7
0.827 0.120 7 99161494 intergenic variant C/A snv 0.67 1