Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs114558062 0.851 0.040 3 187923342 intergenic variant T/C snv 6.6E-03 5
rs11757201 0.851 0.040 6 137682685 intron variant G/C;T snv 5
rs55984493 0.851 0.040 13 99118074 intergenic variant A/T snv 0.15 5
rs970987 0.851 0.040 9 21585266 regulatory region variant C/A snv 0.55 5
rs10202630 0.882 2 190398199 intergenic variant T/C snv 0.52 4
rs10986284 0.882 9 124236874 intergenic variant A/T snv 0.27 4
rs145268310 0.882 3 12269274 regulatory region variant G/C snv 9.9E-02 4
rs1549922 0.882 5 159304540 intergenic variant G/A snv 0.56 4
rs1921445 0.882 3 106229671 intergenic variant A/C;G snv 4
rs221781 0.882 7 100698285 upstream gene variant A/G;T snv 4
rs391851 0.882 5 103342219 intergenic variant A/C;G;T snv 4
rs57791671 0.882 3 121889586 upstream gene variant T/A snv 0.38 4
rs9356551 0.882 6 166986857 intron variant T/C snv 0.42 4
rs9683415 0.882 4 40290296 regulatory region variant A/G snv 0.71 4
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17 14
rs78534766
ADCY7
0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03 7
rs2066363
ADGRL2
0.724 0.240 1 81771892 intron variant C/T snv 0.71 14
rs191252491
ALDH2
0.882 12 111773070 intron variant A/T snv 7.1E-03 4
rs7100025
ANKRD30A ; LINC00993
0.724 0.240 10 37303610 intron variant G/A snv 0.68 14
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30 15
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs1530687
ARHGAP31
0.882 3 119395668 intron variant G/A snv 0.46 4
rs71508903
ARID5B
0.807 0.160 10 62020112 intron variant C/T snv 0.15 7
rs36001488
ATG16L1
0.724 0.240 2 233276621 intron variant C/T snv 0.44 14
rs12928404
ATXN2L
0.724 0.240 16 28835925 splice region variant T/C snv 0.44 0.45 15