Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12423664 | 1.000 | 0.040 | 12 | 132493308 | intron variant | G/A | snv | 0.10 | 6 | ||
rs1250229 | 1.000 | 0.040 | 2 | 215439661 | upstream gene variant | T/C | snv | 0.77 | 3 | ||
rs12740374 | 0.851 | 0.040 | 1 | 109274968 | 3 prime UTR variant | G/T | snv | 0.22 | 9 | ||
rs1800978 | 1.000 | 0.040 | 9 | 104903697 | 5 prime UTR variant | C/A;G;T | snv | 5.4E-06; 0.14 | 6 | ||
rs186696265 | 0.882 | 0.040 | 6 | 160690668 | intergenic variant | C/T | snv | 1.0E-02 | 6 | ||
rs247616 | 1.000 | 0.040 | 16 | 56955678 | intergenic variant | C/T | snv | 0.29 | 6 | ||
rs507666 | 1.000 | 0.040 | 9 | 133273983 | intron variant | A/G | snv | 6 | |||
rs6544713 | 0.925 | 0.040 | 2 | 43846742 | non coding transcript exon variant | T/C | snv | 0.75 | 3 | ||
rs668948 | 1.000 | 0.040 | 2 | 21068657 | regulatory region variant | G/A | snv | 0.71 | 4 | ||
rs895953 | 1.000 | 0.040 | 12 | 121811142 | intron variant | G/T | snv | 0.76 | 5 | ||
rs10738607 | 0.925 | 0.080 | 9 | 22088095 | intron variant | A/G | snv | 0.42 | 3 | ||
rs6982502 | 0.882 | 0.080 | 8 | 125467120 | intron variant | C/T | snv | 0.62 | 4 | ||
rs74617384 | 0.925 | 0.080 | 6 | 160576086 | intron variant | A/G;T | snv | 5 | |||
rs7528419 | 0.851 | 0.080 | 1 | 109274570 | 3 prime UTR variant | A/G | snv | 0.23 | 9 | ||
rs4299376 | 0.851 | 0.120 | 2 | 43845437 | intron variant | G/C;T | snv | 6 | |||
rs6511720 | 0.790 | 0.120 | 19 | 11091630 | intron variant | G/T | snv | 0.12 | 7 | ||
rs1169288 | 0.776 | 0.160 | 12 | 120978847 | missense variant | A/C;T | snv | 0.35 | 8 | ||
rs2244608 | 0.882 | 0.160 | 12 | 120979185 | intron variant | A/G | snv | 0.29 | 6 | ||
rs2954029 | 0.807 | 0.160 | 8 | 125478730 | intron variant | A/T | snv | 0.42 | 7 | ||
rs515135 | 0.807 | 0.160 | 2 | 21063185 | intergenic variant | T/C | snv | 0.73 | 3 | ||
rs2519093 | 0.882 | 0.200 | 9 | 133266456 | intron variant | T/C | snv | 14 | |||
rs1378942 | 0.790 | 0.240 | 15 | 74785026 | intron variant | C/A;T | snv | 6 | |||
rs17696736 | 0.827 | 0.240 | 12 | 112049014 | intron variant | A/G | snv | 0.30 | 12 | ||
rs1800775 | 0.790 | 0.240 | 16 | 56961324 | upstream gene variant | C/A;G | snv | 0.51; 5.7E-06 | 4 | ||
rs646776 | 0.752 | 0.240 | 1 | 109275908 | downstream gene variant | C/T | snv | 0.74 | 10 |