Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10124907 1.000 0.120 9 25659639 intergenic variant A/G;T snv 1
rs11027293 1.000 0.120 11 23530907 intergenic variant T/G snv 2.4E-02 1
rs11256017 1.000 0.120 10 9001956 intergenic variant T/A;C snv 1
rs12973620 1.000 0.120 19 57738275 intron variant G/C snv 0.16 1
rs1332366 1.000 0.120 9 75217659 intergenic variant G/A snv 0.15 1
rs1893361 1.000 0.120 11 74688380 downstream gene variant G/A snv 0.20 1
rs2061 1.000 0.120 17 15157487 regulatory region variant C/A;T snv 2.8E-04 1
rs2606618 1.000 0.120 6 122095195 intergenic variant T/G snv 0.19 1
rs2823048 1.000 0.120 21 15089947 intergenic variant A/G snv 0.18 1
rs2823053 1.000 0.120 21 15092828 intergenic variant A/G snv 0.27 1
rs28361986 1.000 0.120 11 118822452 downstream gene variant T/A snv 5.7E-02 1
rs6583203 1.000 0.120 3 197352715 intergenic variant T/C snv 0.36 1
rs6583337 1.000 0.120 7 40483 upstream gene variant G/A snv 0.35 1
rs7287939 1.000 0.120 22 41000349 intergenic variant T/C snv 5.0E-02 1
rs7780001 1.000 0.120 7 19438358 intron variant A/T snv 0.17 1
rs7824993 1.000 0.120 8 80350661 intron variant A/G snv 0.62 1
rs2472448
ABCA1
1.000 0.120 9 104842226 intron variant C/T snv 0.11 1
rs35350651
ATXN2
1.000 0.120 12 111469627 3 prime UTR variant -/C ins 0.66 1
rs1504215
BACH2 ; LOC105377891
1.000 0.120 6 90296508 5 prime UTR variant G/A;C snv 1
rs2149039
BSND
1.000 0.120 1 55014701 3 prime UTR variant A/C;T snv 1
rs6738964
DAW1
1.000 0.120 2 227874419 intron variant G/A;T snv 1
rs62257549
DCAF1
1.000 0.120 3 51488660 intron variant G/A snv 0.16 1
rs2884670
DYRK4
1.000 0.120 12 4566052 intron variant A/G;T snv 1
rs11677002
FOSL2 ; FLJ31356
1.000 0.120 2 28391534 intron variant T/C snv 0.39 1
rs1373976132
HNMT
1.000 0.120 2 137964586 missense variant T/C snv 4.0E-06 1