Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 34 | |
rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 4 | |
rs301807 | 0.925 | 0.080 | 1 | 8424763 | intron variant | A/G;T | snv | 4 | |||
rs301819 | 0.882 | 0.120 | 1 | 8441726 | intron variant | A/G;T | snv | 3 | |||
rs78037977 | 0.925 | 0.120 | 1 | 172746562 | upstream gene variant | A/G | snv | 7.9E-02 | 2 | ||
rs16843742 | 1.000 | 0.040 | 1 | 198703170 | intron variant | T/C;G | snv | 1 | |||
rs4908760 | 1.000 | 0.040 | 1 | 8466082 | intron variant | G/A | snv | 0.68 | 1 | ||
rs2111485 | 0.724 | 0.280 | 2 | 162254026 | regulatory region variant | A/G | snv | 0.46 | 12 | ||
rs10200159 | 1.000 | 0.040 | 2 | 55617974 | non coding transcript exon variant | T/C | snv | 0.14 | 1 | ||
rs16944 | 0.531 | 0.920 | 2 | 112837290 | upstream gene variant | A/G | snv | 0.57 | 1 | ||
rs199559999 | 1.000 | 0.040 | 2 | 191090480 | intron variant | TAC/- | del | 1 | |||
rs231725 | 0.851 | 0.240 | 2 | 203875952 | downstream gene variant | G/A | snv | 0.38 | 1 | ||
rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 1 | ||
rs41342147 | 1.000 | 0.040 | 2 | 241468173 | missense variant | G/A;T | snv | 0.11; 8.0E-06 | 1 | ||
rs4308124 | 1.000 | 0.040 | 2 | 111252909 | intron variant | T/C | snv | 0.44 | 1 | ||
rs1464510 | 0.807 | 0.280 | 3 | 188394766 | intron variant | C/A;T | snv | 2 | |||
rs13076312 | 1.000 | 0.040 | 3 | 188371466 | intron variant | C/T | snv | 0.44 | 1 | ||
rs148136154 | 1.000 | 0.040 | 3 | 119564621 | intergenic variant | T/C;G | snv | 1 | |||
rs34346645 | 1.000 | 0.040 | 3 | 71508794 | intron variant | C/A | snv | 0.32 | 1 | ||
rs35161626 | 1.000 | 0.040 | 3 | 23470822 | intron variant | A/- | del | 0.64 | 1 | ||
rs59374417 | 0.925 | 0.040 | 3 | 119569567 | intergenic variant | A/C;T | snv | 1 | |||
rs6583331 | 1.000 | 0.040 | 3 | 196620382 | intergenic variant | T/A | snv | 0.38 | 1 | ||
rs9851967 | 1.000 | 0.040 | 3 | 188369840 | intron variant | C/T | snv | 0.35 | 1 | ||
rs16872571 | 0.925 | 0.080 | 4 | 10725229 | intergenic variant | C/T | snv | 0.33 | 2 | ||
rs1031034 | 1.000 | 0.040 | 4 | 101302229 | intron variant | C/A | snv | 0.29 | 1 |