Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs67927699
PUS10
0.882 2 60960280 intron variant G/C;T snv 4
rs7005834
CCN4
0.827 0.160 8 133201961 intron variant C/A;T snv 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
rs78534766
ADCY7
0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03 7
rs114558062 0.851 0.040 3 187923342 intergenic variant T/C snv 6.6E-03 5
rs191252491
ALDH2
0.882 12 111773070 intron variant A/T snv 7.1E-03 4
rs114846446
LINC01250
0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 14
rs117372389
NKD1
0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02 14
rs17466626
LOC105369736 ; LRRK2
0.724 0.240 12 40366829 non coding transcript exon variant A/G snv 1.7E-02 14
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs114378220
CAMK4
0.851 0.040 5 111230662 intron variant C/T snv 4.5E-02 5
rs11622435
LOC101928462
0.827 0.120 14 81151652 intron variant G/A snv 4.7E-02 7
rs9591325
DLEU1
0.851 0.080 13 50237084 intron variant T/C snv 6.0E-02 5
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
rs10494079
VAV3
0.882 1 107832253 intron variant G/C snv 9.0E-02 4
rs145268310 0.882 3 12269274 regulatory region variant G/C snv 9.9E-02 4
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 10
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs35776863
NEURL4
0.882 17 7323638 intron variant G/A snv 0.14 0.14 4