Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11676922
AFF3
0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs32477 1.000 0.080 5 100796873 intergenic variant C/G snv 9.4E-02 1
rs12048904 1.000 0.080 1 100865980 intergenic variant T/C snv 0.48 1
rs11581062
SLC30A7 ; HNRNPA1P68
1.000 0.080 1 100941963 non coding transcript exon variant A/G snv 0.28 1
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 2
rs771767 1.000 0.080 3 102029794 regulatory region variant A/G snv 0.70 1
rs2744148 1.000 0.080 16 1023552 intergenic variant A/G snv 0.15 1
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs7665090
MANBA
0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 1
rs228614
MANBA
0.925 0.120 4 102657480 intron variant G/A snv 0.50 1
rs7924357
WTAPP1
1.000 0.080 11 102757321 intron variant G/A snv 7.9E-02 1
rs10492972
KIF1B
1.000 0.080 1 10293054 intron variant T/C snv 0.32 1
rs26232
MACIR
0.925 0.160 5 103261019 intron variant C/T snv 0.30 4
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 4
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 3
rs8112449
CDC37
0.925 0.160 19 10409388 intron variant G/A snv 0.31 2
rs733724
HACE1
1.000 0.080 6 104775989 intron variant G/A snv 6.1E-02 1
rs9657904
CBLB ; LOC107986109
0.925 0.160 3 105867870 intron variant T/A;C snv 1
rs7746082 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 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
rs11860603
CLEC16A
1.000 0.080 16 11071160 intron variant T/C snv 0.41 1
rs11865121
CLEC16A
1.000 0.080 16 11072831 intron variant C/A snv 0.40 1
rs725613
CLEC16A
0.851 0.240 16 11075826 intron variant T/G snv 0.42 2
rs2041670
CLEC16A
0.851 0.280 16 11080795 intron variant G/A;C snv 2