Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10760279 9 123343012 regulatory region variant G/T snv 0.35 1
rs10760678 9 99317659 intergenic variant G/A snv 0.34 1
rs10764256 10 20616340 intergenic variant C/T snv 0.20 1
rs10773411 12 127560955 upstream gene variant G/A snv 0.31 1
rs10777237 12 90249747 intergenic variant T/A;C snv 1
rs10792006 11 68954837 intergenic variant T/A;C snv 1
rs10797987 1 184682688 intergenic variant T/A;C snv 1
rs10799778 1 22986860 intergenic variant T/G snv 0.74 1
rs10803762 2 160249365 intron variant G/A;C snv 1
rs10804189 2 211124256 intergenic variant A/G snv 0.72 1
rs10811901 9 23356937 intron variant G/A;T snv 1
rs10840606 11 2213460 intergenic variant A/G snv 0.13 1
rs10861861 12 108042619 intergenic variant T/G snv 0.33 1
rs10862426 12 82034979 intergenic variant C/A;G snv 1
rs10871589 18 65618547 intron variant G/A;T snv 1
rs10883027 10 98038477 TF binding site variant G/C snv 0.50 1
rs10905682 10 10216524 intergenic variant C/T snv 0.74 1
rs10937094 3 182579269 intergenic variant A/G snv 0.26 1
rs10942474 5 86868616 intergenic variant A/T snv 0.43 1
rs10947487 6 34221835 downstream gene variant A/G snv 0.88 1
rs10954968 8 34630556 intergenic variant A/G snv 0.36 1
rs10984732 9 119866792 intergenic variant C/T snv 0.27 1
rs10985968 9 123331877 intergenic variant C/G snv 0.53 1
rs11056875 12 16317984 intergenic variant T/C snv 0.79 1
rs11057072 12 16780406 intron variant A/G snv 0.16 1