Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 24 | ||
rs2247056 | 0.882 | 0.160 | 6 | 31297713 | intron variant | T/C | snv | 0.80 | 8 | ||
rs185819 | 0.851 | 0.200 | 6 | 32082290 | missense variant | T/A;C;G | snv | 8.2E-06; 0.58; 4.1E-06 | 8 | ||
rs2516448 | 0.827 | 0.120 | 6 | 31422633 | intron variant | T/C;G | snv | 7 | |||
rs13437082 | 1.000 | 6 | 31386783 | upstream gene variant | C/T | snv | 0.32 | 6 | |||
rs17782313 | 0.683 | 0.480 | 18 | 60183864 | intergenic variant | T/C | snv | 0.24 | 6 | ||
rs6570507 | 0.827 | 0.240 | 6 | 142358435 | intron variant | G/A | snv | 0.47 | 6 | ||
rs6457620 | 0.882 | 0.200 | 6 | 32696222 | intergenic variant | G/C | snv | 0.52 | 4 | ||
rs864745 | 0.763 | 0.320 | 7 | 28140937 | intron variant | T/C | snv | 0.41 | 4 | ||
rs2284746 | 1 | 16980180 | intron variant | C/A;G | snv | 4 | |||||
rs11891311 | 2 | 233730664 | intron variant | G/A | snv | 0.42 | 4 | ||||
rs17391694 | 0.882 | 0.120 | 1 | 78157942 | regulatory region variant | C/T | snv | 7.8E-02 | 3 | ||
rs2844479 | 0.925 | 0.200 | 6 | 31605179 | intergenic variant | A/C | snv | 0.34 | 3 | ||
rs6959212 | 7 | 38088724 | intergenic variant | T/C;G | snv | 3 | |||||
rs7763064 | 6 | 142476152 | intergenic variant | G/A | snv | 0.38 | 3 | ||||
rs3748069 | 6 | 142446496 | downstream gene variant | A/G | snv | 0.39 | 3 | ||||
rs4896582 | 6 | 142382740 | intron variant | G/A | snv | 0.50 | 3 | ||||
rs7741741 | 0.925 | 0.040 | 6 | 142334664 | intron variant | T/A;G | snv | 3 | |||
rs10946808 | 1.000 | 0.040 | 6 | 26233159 | non coding transcript exon variant | A/G | snv | 0.26 | 3 | ||
rs314277 | 0.925 | 0.080 | 6 | 104959787 | intron variant | A/C;G;T | snv | 3 | |||
rs5742915 | 0.925 | 0.080 | 15 | 74044292 | missense variant | T/C;G | snv | 0.35; 4.0E-06 | 3 | ||
rs2417940 | 12 | 20864941 | intron variant | T/A;C | snv | 3 | |||||
rs11024739 | 11 | 18624296 | intron variant | C/A;G | snv | 3 | |||||
rs4148323 | 0.701 | 0.440 | 2 | 233760498 | missense variant | G/A | snv | 2.2E-02 | 9.2E-03 | 3 | |
rs1659127 | 16 | 14294448 | intergenic variant | G/A;C;T | snv | 2 |