Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13415583
AFF3
1.000 0.120 2 100147625 intron variant T/G snv 0.37 1
rs941576
MEG3
1.000 0.120 14 100839708 intron variant A/G snv 0.45 1
rs56994090
MEG3
1.000 0.120 14 100840110 intron variant T/A;C snv 1
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 2
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 7
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 3
rs28641753 0.925 0.160 3 104256574 intergenic variant C/T snv 4.5E-02 2
rs62131887 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 14
rs9810233 0.925 0.200 3 105292046 intergenic variant A/G snv 0.25 2
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
rs17229044
CLEC16A
1.000 0.120 16 10969079 intron variant C/T snv 0.16 1
rs725613
CLEC16A
0.851 0.240 16 11075826 intron variant T/G snv 0.42 1
rs2041670
CLEC16A
0.851 0.280 16 11080795 intron variant G/A;C snv 1
rs7200786
CLEC16A
0.882 0.200 16 11083944 intron variant A/G snv 0.59 2
rs4849135
ACOXL
1.000 0.120 2 110857502 intron variant T/G snv 0.67 1
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 1
rs12924729
CLEC16A
0.882 0.200 16 11093926 intron variant G/A snv 0.34 2
rs12599402
CLEC16A
0.925 0.160 16 11096031 intron variant T/C snv 0.51 1
rs12927355
CLEC16A
0.882 0.240 16 11100914 intron variant C/A;T snv 0.29 2
rs1265564
CUX2
1.000 0.120 12 111270654 non coding transcript exon variant A/C snv 0.30 4
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs2903692
CLEC16A
0.807 0.360 16 11144926 intron variant G/A snv 0.33 1