Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2234253 | 0.827 | 0.120 | 6 | 41161367 | missense variant | G/A;C;T | snv | 1.9E-04; 1.0E-02 | 5 | ||
rs1133763 | 0.882 | 0.200 | 17 | 34320812 | missense variant | A/C | snv | 0.21 | 0.15 | 4 | |
rs63750541 | 0.851 | 0.160 | 17 | 44351586 | missense variant | G/A;C | snv | 8.4E-04 | 4 | ||
rs63751243 | 0.882 | 0.160 | 17 | 44349190 | missense variant | C/A;T | snv | 4.0E-06 | 4 | ||
rs753070659 | 0.851 | 0.160 | 17 | 44350481 | missense variant | G/A;C | snv | 1.2E-05 | 4 | ||
rs763841075 | 0.851 | 0.120 | 17 | 44350293 | missense variant | T/C | snv | 1.8E-04 | 1.1E-04 | 4 | |
rs63750129 | 0.882 | 0.120 | 17 | 45996612 | missense variant | A/C | snv | 4.0E-06 | 4 | ||
rs747019990 | 0.851 | 0.120 | 20 | 4699336 | missense variant | C/T | snv | 3.6E-05 | 7.0E-06 | 4 | |
rs63751180 | 0.882 | 0.120 | 17 | 44352087 | stop gained | C/A;G;T | snv | 4.0E-06; 4.0E-06 | 3 | ||
rs10814083 | 0.882 | 0.160 | 9 | 34256349 | synonymous variant | C/T | snv | 0.40 | 0.34 | 3 | |
rs63750092 | 0.882 | 0.120 | 17 | 46014277 | missense variant | A/T | snv | 3 | |||
rs1163763 | 0.925 | 0.120 | 12 | 17567834 | intron variant | G/T | snv | 0.24 | 2 | ||
rs1052352 | 0.925 | 0.120 | 16 | 31183958 | synonymous variant | C/T | snv | 0.53 | 0.45 | 2 | |
rs741810 | 0.925 | 0.120 | 16 | 31182621 | synonymous variant | C/A;G;T | snv | 0.32; 4.0E-06; 4.0E-06 | 2 | ||
rs752076094 | 0.925 | 0.120 | 16 | 31185175 | missense variant | A/G | snv | 8.4E-06 | 2.8E-05 | 2 | |
rs533451404 | 0.925 | 0.120 | 17 | 44349267 | missense variant | G/A | snv | 1.6E-05 | 2.1E-05 | 2 | |
rs536551654 | 1.000 | 0.120 | 17 | 49511972 | missense variant | T/C | snv | 2 | |||
rs1319062081 | 0.925 | 0.120 | 21 | 31668537 | stop gained | G/T | snv | 2 | |||
rs706118 | 1.000 | 0.120 | 9 | 33256181 | intron variant | T/G | snv | 0.39 | 1 | ||
rs1415210991 | 1.000 | 0.120 | 11 | 27701003 | 5 prime UTR variant | G/C | snv | 4.2E-06 | 1 | ||
rs1431475678 | 1.000 | 0.120 | 11 | 27658555 | missense variant | G/C | snv | 7.0E-06 | 1 | ||
rs4859147 | 1.000 | 0.120 | 3 | 182964065 | intron variant | T/C | snv | 0.56 | 0.48 | 1 | |
rs1417841099 | 1.000 | 0.120 | 19 | 852917 | missense variant | C/G | snv | 4.6E-06 | 1 | ||
rs750810467 | 1.000 | 0.120 | 17 | 44351420 | missense variant | G/A;C | snv | 4.8E-05; 4.0E-06 | 1 | ||
rs7967622 | 1.000 | 0.120 | 12 | 54284196 | intron variant | C/T | snv | 0.76 | 1 |