Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17266594
BANK1
0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 1
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 2
rs4622329
DRAM1
1.000 0.080 12 101928157 intron variant G/A snv 0.46 1
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 4
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 2
rs280519
TYK2
0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 2
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 3
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 4
rs6568431
ATG5
0.790 0.320 6 106140931 intron variant A/C snv 0.61 2
rs3827644
ATG5
0.925 0.080 6 106237320 intron variant G/C snv 0.15 1
rs573775
ATG5
0.851 0.320 6 106316991 intron variant G/A snv 0.34 1
rs4956211 1.000 0.080 4 108801970 intergenic variant G/A snv 0.37 1
rs6985109
XKR6
1.000 0.080 8 10904075 intron variant G/A;C;T snv 1
rs4240671
XKR6
1.000 0.080 8 10910238 intron variant G/A snv 0.49 1
rs11783247
XKR6
1.000 0.080 8 10931365 intron variant C/T snv 0.54 1
rs6984496
XKR6
1.000 0.080 8 10938583 intron variant G/T snv 0.56 1
rs2041670
CLEC16A
0.851 0.280 16 11080795 intron variant G/A;C snv 2
rs7200786
CLEC16A
0.882 0.200 16 11083944 intron variant A/G snv 0.59 2
rs12599402
CLEC16A
0.925 0.160 16 11096031 intron variant T/C snv 0.51 2
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 4
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs33980500
TRAF3IP2-AS1 ; TRAF3IP2
0.742 0.200 6 111592059 missense variant C/T snv 8.6E-02 9.7E-02 2
rs17630235
TRAFD1
0.925 0.120 12 112153882 downstream gene variant G/A;C snv 3
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 4
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6