Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 10
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20 6
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 6
rs61894547
EMSY
0.882 0.160 11 76537586 intron variant C/T snv 3.1E-02 4
rs4671393
BCL11A
0.790 0.400 2 60493816 intron variant A/C;G snv 3
rs1986734
SHROOM3
1.000 0.120 4 76499631 intron variant C/T snv 0.43 3
rs11495981
JAZF1
1.000 0.120 7 28137682 intron variant C/T snv 0.29 2
rs167769
STAT6
0.827 0.280 12 57109992 5 prime UTR variant C/T snv 0.31 2
rs11819199 1.000 0.120 10 20576228 intergenic variant A/G snv 0.12 1
rs2000260 1.000 0.120 1 108130783 downstream gene variant A/G snv 0.37 1
rs2055376 1.000 0.120 5 116845732 regulatory region variant G/A;T snv 1
rs252716 1.000 0.120 5 111089365 intron variant G/A;C snv 1
rs599707 0.925 0.200 6 31840659 downstream gene variant C/T snv 7.6E-02 1
rs6799767 1.000 0.120 3 176312308 intergenic variant G/A;T snv 1
rs8041227 1.000 0.120 15 31246339 intergenic variant G/A snv 0.18 1
rs3815700
ANKRD27
1.000 0.120 19 32602346 intron variant T/C snv 0.19 1
rs149864795
CAPN14
1.000 0.120 2 31179541 intron variant G/A snv 4.8E-02 1
rs77569859
CAPN14
1.000 0.120 2 31188421 intron variant T/C snv 4.1E-02 1
rs77301713
CAPN5
1.000 0.120 11 77121400 intron variant G/A snv 2.0E-02 1
rs118086209
CCDC81
1.000 0.120 11 86393453 intron variant T/C;G snv 1
rs3744790
CEP295NL ; TIMP2
1.000 0.120 17 78897053 intron variant C/T snv 0.14 1
rs12924112
CLEC16A
1.000 0.120 16 11125863 intron variant T/A;G snv 1
rs9956738
DCC
1.000 0.120 18 52414603 intron variant A/G snv 4.6E-02 1
rs28530674
IFFO2
1.000 0.120 1 18907640 3 prime UTR variant A/G snv 0.11 1
rs2296225
KIF17
0.882 0.160 1 20704549 missense variant T/C;G snv 0.12; 4.0E-06 1