Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs191252491
ALDH2
0.882 12 111773070 intron variant A/T snv 7.1E-03 4
rs1530687
ARHGAP31
0.882 3 119395668 intron variant G/A snv 0.46 4
rs1320344
C12orf42
0.882 12 103493699 intron variant A/G snv 0.64 4
rs1199047
CCDC88B
0.882 11 64350711 intron variant A/C snv 0.38 4
rs7005834
CCN4
0.827 0.160 8 133201961 intron variant C/A;T snv 4
rs1790588
CD226
0.882 18 69867948 intron variant T/C snv 0.55 4
rs56817615
CLNK
0.882 4 10717222 intergenic variant A/G snv 0.42 4
rs12980063
CPT1C
0.882 19 49693735 intron variant A/G snv 0.48 4
rs6840978
IL21-AS1
0.776 0.160 4 122633552 intron variant C/T snv 0.16 4
rs72920202
JAK1
0.882 1 64895266 intron variant A/T snv 0.15 4
rs142647938
KCNH7
0.882 2 162516642 intron variant C/A;T snv 4
rs11785816
LINC00824
0.882 8 128518940 intron variant C/A;G snv 4
rs2093816
LINC02341
0.882 13 42471900 intron variant C/T snv 0.47 4
rs2181622
LINC02656 ; LINC02649
0.882 10 6349099 intron variant G/A snv 0.59 4
rs8061370
LOC105371082 ; RMI2
0.882 16 11364614 intron variant A/C;T snv 4