Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10039206 5 56692951 intergenic variant T/C snv 0.61 2
rs10159676 10 50302023 downstream gene variant G/A snv 0.34 2
rs10223451 6 139630553 intron variant A/G snv 0.58 2
rs1029555 7 26547477 upstream gene variant T/C snv 0.80 2
rs10410869 19 57629913 upstream gene variant G/T snv 0.12 2
rs10424080 19 18407968 TF binding site variant C/T snv 0.29 2
rs10883353 10 99496351 intergenic variant G/A snv 0.82 2
rs10897221 11 62171647 downstream gene variant G/T snv 0.22 2
rs10898438 11 86147211 intergenic variant G/A;C snv 2
rs10923398 1 117708553 regulatory region variant A/C snv 0.16 2
rs10971957 9 34151465 regulatory region variant C/T snv 0.51 2
rs10991473 9 105024605 downstream gene variant G/A;C snv 2
rs11117363 16 88086625 intron variant A/C;G snv 2
rs111527163 4 68732288 intergenic variant A/T snv 0.19 2
rs112421097 4 68870942 intergenic variant A/G snv 5.5E-02 2
rs113617776 6 135165003 intergenic variant G/A snv 9.4E-03 2
rs113954756 11 123066748 intron variant G/A snv 0.13 2
rs1155998 8 97639920 upstream gene variant C/A snv 0.22 2
rs117129959 11 15957881 regulatory region variant T/A snv 4.1E-03 2
rs117338687 11 61671194 regulatory region variant G/C snv 5.7E-03 2
rs11750130 5 154641024 intergenic variant A/G snv 0.36 2
rs11769676 7 129569211 regulatory region variant G/A snv 0.31 2
rs117893233 5 1041318 downstream gene variant C/T snv 2.6E-03 2
rs11799474 1 22377698 intergenic variant T/G snv 0.20 2
rs11845708 14 23046166 downstream gene variant C/T snv 0.28 2