Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10922907 1 90727492 downstream gene variant A/G;T snv 2
rs10937921 1.000 0.120 4 3274764 downstream gene variant C/T snv 0.40 2
rs12761761
PPP2R2D
10 131961871 downstream gene variant C/T snv 0.21 2
rs2726513
TET2-AS1
4 105296201 downstream gene variant G/T snv 0.37 2
rs4484297 4 16330759 downstream gene variant G/C snv 0.31 2
rs5757673 22 39441915 downstream gene variant T/C snv 0.79 2
rs6949851 7 32454195 downstream gene variant T/G snv 0.33 2
rs10040865
NPM1
5 171411280 downstream gene variant G/A snv 0.40 1
rs10064431
FAM172A
5 93614967 downstream gene variant T/C snv 0.41 1
rs1016678 17 37514090 downstream gene variant A/G snv 0.72 1
rs10211312
LOC105374764 ; TMEM17
2 62466982 downstream gene variant A/C;T snv 1
rs1073090 1 96023656 downstream gene variant G/A snv 0.17 1
rs10819655 9 99352018 downstream gene variant A/T snv 0.37 1
rs10911009 1 182052669 downstream gene variant C/T snv 0.24 1
rs11081529 18 78142735 downstream gene variant T/C snv 0.31 1
rs111683602 19 12979602 downstream gene variant A/G snv 0.15 1
rs1147198 9 84660433 downstream gene variant G/T snv 0.70 1
rs116674558 1 98078517 downstream gene variant G/A snv 2.2E-02 1
rs11880195 19 49632177 downstream gene variant C/G;T snv 1
rs11914869 3 82465761 downstream gene variant T/A snv 1.0E-02 1
rs12032969
LINC02238
1 73718667 downstream gene variant T/C snv 0.27 1
rs12735006 1 164900632 downstream gene variant A/G snv 0.17 1
rs1413422 20 58005891 downstream gene variant T/C snv 0.60 1
rs1490612 4 105489698 downstream gene variant G/T snv 5.8E-02 1
rs1693584
LOC105375673
8 100736689 downstream gene variant T/C snv 0.28 1