Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11571297 0.882 0.120 2 203880280 regulatory region variant T/C snv 0.44 3
rs13093110
LPP
0.882 0.120 3 188407332 intron variant C/T snv 0.42 3
rs57348955 0.882 0.120 16 31174561 upstream gene variant G/A;C snv 3
rs7537605
VAV3
0.882 0.120 1 107800465 intron variant G/A;T snv 3
rs1015166
TAP2
0.925 0.120 6 32830954 intron variant C/G;T snv 0.28 2
rs2358994
BCL2L15 ; AP4B1-AS1
0.925 0.120 1 113886839 intron variant G/A snv 0.16 2
rs7679475
LOC107986309
0.925 0.120 4 121392885 intergenic variant A/C;G snv 2
rs1534422
MIR3681HG
0.827 0.160 2 12500615 intron variant G/A snv 0.52 4
rs706779
IL2RA
0.827 0.160 10 6056861 intron variant T/C snv 0.48 4
rs2270450
LOC101926934 ; SLC25A27
0.827 0.200 6 46677138 3 prime UTR variant C/T snv 0.29 3
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs1689510
SUOX
0.724 0.240 12 56002984 non coding transcript exon variant G/C snv 0.25 16
rs12598357 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 15
rs12928404
ATXN2L
0.724 0.240 16 28835925 splice region variant T/C snv 0.44 0.45 15
rs2836882 0.724 0.240 21 39094644 intergenic variant G/A snv 0.23 15
rs36051895 0.716 0.240 9 4981866 upstream gene variant G/T snv 0.25 15
rs62324212
IL21-AS1
0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 15
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30 15
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14
rs10988542
FNBP1
0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs114846446
LINC01250
0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 14
rs11580078
C1orf141 ; IL23R
0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs117372389
NKD1
0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02 14