Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10783124 1.000 0.080 1 99937719 intergenic variant A/G snv 2.9E-02 1
rs112407915 1.000 0.080 3 5505762 intergenic variant T/A snv 1.6E-02 1
rs114425659 1.000 0.080 4 117920116 intergenic variant G/A snv 4.9E-02 1
rs115747230 1.000 0.080 9 76994030 downstream gene variant T/C snv 1.8E-02 1
rs11645800 1.000 0.080 16 62966386 intergenic variant A/G snv 0.19 1
rs116510623 1.000 0.080 11 24209937 intergenic variant A/G snv 2.6E-02 1
rs12963285 1.000 0.080 18 57097183 intergenic variant T/C snv 0.10 1
rs13084795 1.000 0.080 3 152612677 intergenic variant G/A snv 0.19 1
rs1505141 1.000 0.080 13 76307915 intergenic variant C/G snv 0.50 1
rs187652497 1.000 0.080 21 41628325 regulatory region variant T/C snv 7.4E-03 1
rs191540116 1.000 0.080 17 14286592 intergenic variant G/A snv 1.3E-02 1
rs1989248 1.000 0.080 7 148443990 upstream gene variant A/C;G snv 1
rs2681019 1.000 0.080 2 22964632 intergenic variant C/A snv 0.61 1
rs4821469 1.000 0.080 22 36220399 intergenic variant T/C snv 0.21 1
rs594442 1.000 0.080 6 93138166 intergenic variant A/C;T snv 1
rs6816344 1.000 0.080 4 72917687 intergenic variant A/T snv 0.36 1
rs76064236 1.000 0.080 1 226335330 upstream gene variant T/G snv 2.1E-03 1
rs77138376 1.000 0.080 1 78168337 downstream gene variant G/A;C snv 1
rs8050506 1.000 0.080 16 54379818 intergenic variant G/A snv 0.18 1
rs926392 1.000 0.080 20 39061821 intergenic variant A/G;T snv 1
rs138873021
ADCY8
1.000 0.080 8 130951170 intron variant AGA/- delins 0.68 1
rs7562121
AFF3
1.000 0.080 2 99767892 intron variant C/G snv 0.66 1
rs138572244
C22orf31
1.000 0.080 22 29065297 upstream gene variant G/A snv 6.6E-03 1
rs815815
CALM2
1.000 0.080 2 47171925 non coding transcript exon variant C/A;T snv 1
rs553908921
CCSER1
1.000 0.080 4 91329657 intron variant C/T snv 1.4E-05 1