Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7203560
NPRL3
1.000 0.080 16 134391 intron variant T/G snv 2.0E-02 6
rs10189857
BCL11A
1.000 0.080 2 60486100 intron variant A/G snv 0.42 5
rs766432
BCL11A
0.925 0.080 2 60492835 intron variant C/A snv 0.80 5
rs6729815
BCL11A
1.000 0.080 2 60496537 intron variant T/C snv 0.49 4
rs7606173
BCL11A
1.000 0.080 2 60498316 intron variant G/C;T snv 0.39 4
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 4
rs7565301
BCL11A
1.000 0.080 2 60496131 intron variant G/A snv 0.25 3
rs10172646
BCL11A
1.000 0.080 2 60493622 intron variant G/A snv 0.64 2
rs10195871
BCL11A
1.000 0.080 2 60493454 intron variant A/G;T snv 2
rs11968814 1.000 0.080 6 71067268 intergenic variant G/A snv 4.4E-02 2
rs1318772
MCC
1.000 0.080 5 113387870 intron variant A/G snv 0.18 2
rs1669539 1.000 0.080 2 105998818 intergenic variant T/C snv 7.1E-02 2
rs1896294
BCL11A
1.000 0.080 2 60491939 intron variant C/G;T snv 2
rs1896295
BCL11A
1.000 0.080 2 60496951 intron variant T/C snv 0.81 2
rs1896296
BCL11A
1.000 0.080 2 60496952 intron variant G/T snv 0.80 2
rs6545816
BCL11A
1.000 0.080 2 60487726 intron variant A/C;G snv 0.50 2
rs6545817
BCL11A
1.000 0.080 2 60488044 intron variant C/T snv 0.49 2
rs6706648
BCL11A
1.000 0.080 2 60494905 intron variant C/G;T snv 2
rs67072384
ARAP1
0.925 0.080 11 72739679 intron variant C/T snv 0.14 2
rs6738440
BCL11A
1.000 0.080 2 60495106 intron variant A/G snv 0.26 2
rs7557939
BCL11A
1.000 0.080 2 60494212 intron variant G/A snv 0.64 2
rs7584113
BCL11A
1.000 0.080 2 60494176 intron variant A/G snv 0.64 2
rs75853687
LINC01847
0.925 0.080 5 159850278 intron variant G/A snv 1.7E-02 2
rs7952106 1.000 0.080 11 113553836 regulatory region variant G/T snv 0.71 2
rs144995469 1.000 0.080 14 56732364 upstream gene variant C/T snv 8.6E-03 1