Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs114378220
CAMK4
0.851 0.040 5 111230662 intron variant C/T snv 4.5E-02 5
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs33980500
TRAF3IP2-AS1 ; TRAF3IP2
0.742 0.200 6 111592059 missense variant C/T snv 8.6E-02 9.7E-02 3
rs191252491
ALDH2
0.882 12 111773070 intron variant A/T snv 7.1E-03 4
rs3811047
IL37
0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60 1
rs12928822
LOC105371082 ; RMI2
0.882 0.200 16 11310036 intron variant C/T snv 0.13 1
rs8061370
LOC105371082 ; RMI2
0.882 16 11364614 intron variant A/C;T snv 4
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 2
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 4
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 1
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 5
rs10892258
LOC105369519
0.925 0.120 11 118709156 intron variant G/A snv 0.19 1
rs10892279 1.000 0.120 11 118741072 intron variant G/A;T snv 0.25 3
rs638893 0.882 0.080 11 118827828 intergenic variant G/A snv 0.79 1
rs6421571 0.851 0.200 11 118873063 intergenic variant T/A;C snv 2
rs1032129
TNFRSF11B
0.851 0.040 8 118939661 intron variant A/C snv 0.37 5
rs1530687
ARHGAP31
0.882 3 119395668 intron variant G/A snv 0.46 4
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 1
rs13299616
PSMD5 ; CUTALP
0.882 9 120832525 intron variant T/C snv 0.50 4
rs1953126
PHF19
1.000 0.120 9 120878222 intron variant T/C snv 0.68 2