Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs221781 0.882 7 100698285 upstream gene variant A/G;T snv 4
rs240753
LOC105372548
0.882 20 17881170 intergenic variant T/C snv 0.43 4
rs28583049
LOC105374033
0.882 3 108724568 downstream gene variant T/C snv 0.17 4
rs35776863
NEURL4
0.882 17 7323638 intron variant G/A snv 0.14 0.14 4
rs391851 0.882 5 103342219 intergenic variant A/C;G;T snv 4
rs4761587
PLXNC1
0.882 12 94158023 intron variant A/G snv 0.78 4
rs56817615
CLNK
0.882 4 10717222 intergenic variant A/G snv 0.42 4
rs57791671 0.882 3 121889586 upstream gene variant T/A snv 0.38 4
rs67927699
PUS10
0.882 2 60960280 intron variant G/C;T snv 4
rs72920202
JAK1
0.882 1 64895266 intron variant A/T snv 0.15 4
rs7655915
LOC107986195
0.882 4 148712316 intron variant C/T snv 0.22 4
rs773107
RAB5B
0.882 12 55975722 intron variant A/G;T snv 4
rs8061370
LOC105371082 ; RMI2
0.882 16 11364614 intron variant A/C;T snv 4
rs865488
TG
0.882 8 132926377 intron variant C/T snv 0.67 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
rs76428106
FLT3
0.851 0.040 13 28029870 intron variant T/C;G snv 10
rs10425559 0.807 0.040 19 4837475 upstream gene variant A/G snv 0.66 7
rs3765209
LOC101927745
0.851 0.040 21 15417030 intron variant C/T snv 0.31 7
rs1032129
TNFRSF11B
0.851 0.040 8 118939661 intron variant A/C snv 0.37 5
rs11073337
RASGRP1
0.851 0.040 15 38555562 intron variant A/C snv 0.27 5
rs114378220
CAMK4
0.851 0.040 5 111230662 intron variant C/T snv 4.5E-02 5
rs114558062 0.851 0.040 3 187923342 intergenic variant T/C snv 6.6E-03 5