Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs970987 0.851 0.040 9 21585266 regulatory region variant C/A snv 0.55 5
rs9683415 0.882 4 40290296 regulatory region variant A/G snv 0.71 4
rs9591325
DLEU1
0.851 0.080 13 50237084 intron variant T/C snv 6.0E-02 5
rs9507287
SPATA13
0.851 0.040 13 24212439 intron variant T/C snv 0.24 5
rs9392504 0.827 0.120 6 412802 downstream gene variant G/A snv 0.44 7
rs9356551 0.882 6 166986857 intron variant T/C snv 0.42 4
rs865488
TG
0.882 8 132926377 intron variant C/T snv 0.67 4
rs8061370
LOC105371082 ; RMI2
0.882 16 11364614 intron variant A/C;T snv 4
rs78534766
ADCY7
0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03 7
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30 15
rs773107
RAB5B
0.882 12 55975722 intron variant A/G;T snv 4
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 15
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17 14
rs7672495 0.724 0.240 4 4990640 regulatory region variant T/C snv 0.21 14
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs7655915
LOC107986195
0.882 4 148712316 intron variant C/T snv 0.22 4
rs76428106
FLT3
0.851 0.040 13 28029870 intron variant T/C;G snv 10
rs761357
LINC00271
0.851 0.040 6 135581461 intron variant A/G;T snv 5
rs7568275
STAT4
0.827 0.120 2 191101726 intron variant G/C;T snv 5
rs755374 0.724 0.240 5 159402286 intron variant C/T snv 0.28 14
rs7441808
LINC02357
0.851 0.040 4 26088753 intron variant A/G snv 0.20 5
rs73316435
ITGB3
0.882 17 47252111 upstream gene variant C/A;T snv 5
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19