Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1700159 | 1.000 | 0.040 | 12 | 51912002 | intron variant | C/A;G;T | snv | 4 | |||
rs1811069 | 1.000 | 0.040 | 22 | 21627765 | upstream gene variant | T/A;G | snv | 4 | |||
rs114269697 | 1.000 | 0.040 | 1 | 64848529 | intron variant | C/A | snv | 7.3E-03 | 3 | ||
rs71368508 | 1.000 | 0.040 | 17 | 4618178 | downstream gene variant | C/A | snv | 1.7E-02 | 3 | ||
rs7713145 | 1.000 | 0.040 | 5 | 177354208 | upstream gene variant | G/A | snv | 0.37 | 3 | ||
rs891058 | 1.000 | 0.040 | 2 | 8302417 | non coding transcript exon variant | G/A | snv | 0.23 | 3 | ||
rs10910095 | 1.000 | 0.040 | 1 | 2579316 | upstream gene variant | G/A;C | snv | 2 | |||
rs10947428 | 1.000 | 0.040 | 6 | 33679281 | intron variant | T/C | snv | 0.26 | 2 | ||
rs11242709 | 1.000 | 0.040 | 6 | 209159 | upstream gene variant | C/T | snv | 0.19 | 2 | ||
rs11255753 | 1.000 | 0.040 | 10 | 8563590 | intergenic variant | G/C;T | snv | 0.23 | 2 | ||
rs11539209 | 1.000 | 0.040 | 9 | 128721272 | missense variant | T/A;C | snv | 7.4E-02 | 2 | ||
rs2255088 | 1.000 | 0.040 | 10 | 6583416 | intron variant | T/C | snv | 0.39 | 2 | ||
rs250308 | 1.000 | 0.040 | 5 | 119348602 | intron variant | T/A;C | snv | 2 | |||
rs2744939 | 1.000 | 0.040 | 6 | 34580429 | upstream gene variant | T/A | snv | 0.17 | 2 | ||
rs3856261 | 1.000 | 0.040 | 1 | 155906822 | intron variant | G/A | snv | 0.36 | 2 | ||
rs4580194 | 1.000 | 0.040 | 17 | 39970224 | intron variant | A/G | snv | 0.41 | 2 | ||
rs519973 | 1.000 | 0.040 | 3 | 187915480 | intergenic variant | G/A | snv | 0.33 | 2 | ||
rs59185885 | 1.000 | 0.040 | 2 | 102327786 | intron variant | T/G | snv | 0.18 | 2 | ||
rs60946162 | 1.000 | 0.040 | 3 | 188415548 | intron variant | C/T | snv | 0.35 | 2 | ||
rs61192126 | 1.000 | 0.040 | 3 | 72345701 | intergenic variant | T/C | snv | 0.26 | 2 | ||
rs6785012 | 1.000 | 0.040 | 3 | 141390506 | intron variant | C/T | snv | 0.54 | 2 | ||
rs76167968 | 1.000 | 0.040 | 1 | 35216137 | intergenic variant | T/C | snv | 0.25 | 2 | ||
rs10131567 | 1.000 | 0.040 | 14 | 35395672 | intergenic variant | G/T | snv | 0.22 | 1 | ||
rs10244416 | 1.000 | 0.040 | 7 | 20536128 | intergenic variant | C/A;T | snv | 0.52 | 1 | ||
rs1025549 | 1.000 | 0.040 | 2 | 198016459 | intron variant | G/A;T | snv | 1 |