Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs7655915
LOC107986195
0.882 4 148712316 intron variant C/T snv 0.22 4
rs10444776
LOC112268138
0.882 14 105647030 upstream gene variant G/A;T snv 4
rs10937560
MB21D2
0.882 3 192909627 intron variant G/C snv 0.45 4
rs35776863
NEURL4
0.882 17 7323638 intron variant G/A snv 0.14 0.14 4
rs1800601
NTRK1 ; SH2D2A
0.882 1 156815825 5 prime UTR variant G/A;T snv 0.67; 4.0E-06 4
rs7088058
PLEKHA1
0.851 0.040 10 122389836 intron variant C/T snv 0.32 4
rs4761587
PLXNC1
0.882 12 94158023 intron variant A/G snv 0.78 4
rs13299616
PSMD5 ; CUTALP
0.882 9 120832525 intron variant T/C snv 0.50 4
rs67927699
PUS10
0.882 2 60960280 intron variant G/C;T snv 4
rs773107
RAB5B
0.882 12 55975722 intron variant A/G;T snv 4
rs13380830
RAB5C
0.882 17 42145640 intron variant C/G snv 0.29 4
rs11746555
SLC22A5
0.882 5 132391341 intron variant G/A snv 0.28 4
rs865488
TG
0.882 8 132926377 intron variant C/T snv 0.67 4
rs10494079
VAV3
0.882 1 107832253 intron variant G/C snv 9.0E-02 4
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
rs114378220
CAMK4
0.851 0.040 5 111230662 intron variant C/T snv 4.5E-02 5
rs9591325
DLEU1
0.851 0.080 13 50237084 intron variant T/C snv 6.0E-02 5
rs2075302
FAP
0.882 2 162219636 intron variant T/C snv 0.34 5
rs73316435
ITGB3
0.882 17 47252111 upstream gene variant C/A;T snv 5
rs761357
LINC00271
0.851 0.040 6 135581461 intron variant A/G;T snv 5