Source: GWASCAT ×
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 1
rs7552544 1.000 0.080 1 100775337 intergenic variant T/C snv 0.35 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 1
rs771767 1.000 0.080 3 102029794 regulatory region variant A/G snv 0.70 2
rs1398607 1.000 0.080 3 102036894 TF binding site variant C/A;T snv 2
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 2
rs7665090
MANBA
0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 4
rs228614
MANBA
0.925 0.120 4 102657480 intron variant G/A snv 0.50 2
rs7924357
WTAPP1
1.000 0.080 11 102757321 intron variant G/A snv 7.9E-02 1
rs12148050
TRAF3
1.000 0.080 14 102797451 intron variant A/G snv 0.50 1
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
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 1
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
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 1
rs733724
HACE1
1.000 0.080 6 104775989 intron variant G/A snv 6.1E-02 1
rs2726518
TET2-AS1 ; TET2
1.000 0.080 4 105252042 intron variant A/C snv 0.63 1
rs11621145
IGHA1
1.000 0.080 14 105706543 intron variant G/A snv 0.49 3
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 1