Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs198846
H1-6
6 26107235 downstream gene variant A/G;T snv 7
rs6495122 1.000 0.040 15 74833304 downstream gene variant A/C snv 0.44 6
rs2969070 7 2472910 downstream gene variant G/A;C snv 3
rs13040716 1.000 0.040 20 32182402 downstream gene variant A/G snv 1.0E-01 2
rs4638749 2 108267586 downstream gene variant G/A snv 0.26 2
rs12098903 11 55899037 downstream gene variant A/T snv 5.7E-02 1
rs12098904 11 55899077 downstream gene variant A/T snv 5.7E-02 1
rs12098941 11 55898967 downstream gene variant T/A;G snv 1
rs17510438 11 55902839 downstream gene variant G/A snv 5.7E-02 1
rs17531933 11 56128173 downstream gene variant T/C;G snv 1
rs17531954 11 56128255 downstream gene variant T/C snv 6.0E-02 1
rs17596143 11 55910869 downstream gene variant T/A snv 5.7E-02 1
rs17610514 11 56128322 downstream gene variant A/G snv 6.0E-02 1
rs7929570 11 56109777 downstream gene variant T/C snv 6.0E-02 1
rs7935728 11 56111979 downstream gene variant C/T snv 6.0E-02 1
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs17477177 1.000 0.080 7 106771412 upstream gene variant T/C snv 0.17 4
rs61781370 1.000 0.040 1 39579628 upstream gene variant A/C snv 0.17 2
rs943580 1 230701298 upstream gene variant G/A snv 0.42 2
rs10444602 12 131708291 upstream gene variant T/G snv 0.51 1
rs1384089 11 56081540 upstream gene variant G/C snv 6.0E-02 1
rs17511107 11 55908549 upstream gene variant T/C snv 5.7E-02 1
rs17530228 11 56081680 upstream gene variant A/G snv 6.0E-02 1
rs17598045 11 55940815 upstream gene variant G/A;T snv 1
rs17598094 11 55941339 upstream gene variant T/C snv 6.0E-02 1