Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10421649 19 9831586 upstream gene variant T/A snv 0.52 1
rs10823730 10 71387550 intergenic variant T/C snv 0.43 1
rs10973207 9 37100528 TF binding site variant G/T snv 0.13 1
rs112477743 6 98202301 intron variant T/-;TT;TTT;TTTTTTTTTTT delins 1
rs115578460 1 98597446 intergenic variant C/T snv 2.5E-02 1
rs11654671 17 4829172 upstream gene variant A/G;T snv 1
rs11739656 5 174767801 intron variant C/T snv 0.11 1
rs12441664 15 97171304 intergenic variant A/T snv 0.21 1
rs12518468 5 7249583 intergenic variant T/C snv 0.27 1
rs12567114 1 98062395 intergenic variant G/A snv 0.22 1
rs12611523 2 138437758 intron variant A/G snv 0.43 1
rs1263056 11 116705699 intergenic variant A/G snv 0.60 1
rs12791153 11 80974138 intergenic variant A/T snv 6.2E-02 1
rs142180737 6 28376954 downstream gene variant T/C snv 4.2E-03 1
rs151014368 5 177324058 regulatory region variant G/A snv 0.16 1
rs1633063 6 29758269 intron variant C/T snv 0.20 1
rs16854 13 110103485 intron variant T/A;C snv 1
rs17005118 4 81367410 intergenic variant G/A snv 0.27 1
rs17285646 4 91636345 intergenic variant T/A snv 0.44 1
rs17401208 5 143497144 intron variant A/G snv 3.9E-02 1
rs17427571 4 81333754 upstream gene variant A/G;T snv 1
rs17635531 3 143247876 intergenic variant G/A snv 5.2E-02 1
rs1776776 9 137602620 upstream gene variant T/C snv 0.20 1
rs1784848 18 2176439 intron variant T/C snv 0.98 1
rs2192528 4 18326273 intergenic variant A/G snv 0.61 1