Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1734907 0.925 0.080 7 100717894 upstream gene variant A/G snv 0.84 2
rs13126505
BANK1
1.000 0.040 4 101944147 intron variant G/A snv 4.1E-02 1
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs13001325
IL18R1 ; IL1RL1
1.000 0.040 2 102322576 intron variant C/T snv 0.30 1
rs13015714
IL18R1
0.882 0.200 2 102355405 intron variant G/T snv 0.77 2
rs2058660
IL18RAP
0.882 0.280 2 102437989 intron variant G/A snv 0.78 1
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs7705924
LINC00492 ; LINC00491
1.000 0.040 5 102611094 intron variant A/G snv 5.1E-02 1
rs74956615
FDX2 ; RAVER1
0.807 0.160 19 10317045 3 prime UTR variant T/A;C snv 1
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
rs11879191
CDC37
1.000 0.040 19 10402235 intron variant G/A;C snv 1
rs6568421 1.000 0.040 6 105987150 regulatory region variant A/G snv 0.23 2
rs7746082 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 3
rs12369214
RIC8B
0.807 0.120 12 106804833 intron variant G/A snv 0.41 1
rs12014762
MORC4
0.882 0.080 X 106940440 intron variant C/T snv 0.14 1
rs2930047
DAP
0.925 0.040 5 10695414 intron variant T/C snv 0.49 1
rs6622126
MORC4
0.851 0.080 X 106956972 missense variant G/A snv 0.58 1
rs4561177
RDX ; ZC3H12C
0.807 0.120 11 110091706 intron variant A/G snv 0.36 1
rs11195128 1.000 0.040 10 110426390 downstream gene variant C/G;T snv 1
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs2903692
CLEC16A
0.807 0.360 16 11144926 intron variant G/A snv 0.33 1
rs3851228
LOC107986522 ; TRAF3IP2-AS1
0.925 0.040 6 111526988 intron variant A/T snv 9.7E-02 1
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17