Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2841307 | 6 | 100308811 | intergenic variant | C/T | snv | 0.20 | 2 | ||||
rs2044117 | 13 | 101055958 | intron variant | G/A | snv | 0.19 | 2 | ||||
rs12105421 | 1.000 | 0.040 | 2 | 102959630 | intron variant | C/T | snv | 7.8E-02 | 2 | ||
rs6484218 | 0.882 | 0.040 | 11 | 10369034 | intron variant | G/A | snv | 0.21 | 5 | ||
rs2498804 | 0.827 | 0.160 | 14 | 104766758 | intron variant | C/A;T | snv | 0.40 | 0.33 | 8 | |
rs2494732 | 0.763 | 0.240 | 14 | 104772855 | intron variant | T/C | snv | 0.50 | 0.47 | 11 | |
rs3730358 | 0.724 | 0.360 | 14 | 104780070 | intron variant | G/A;C | snv | 0.16; 4.0E-03 | 14 | ||
rs1130214 | 0.742 | 0.280 | 14 | 104793397 | 5 prime UTR variant | C/A | snv | 0.31 | 12 | ||
rs3803300 | 0.827 | 0.120 | 14 | 104803442 | 3 prime UTR variant | T/A;C | snv | 6 | |||
rs3916965 | 0.882 | 0.040 | 13 | 105451011 | intergenic variant | C/T | snv | 0.31 | 4 | ||
rs1341402 | 1.000 | 0.040 | 13 | 105463160 | intron variant | T/C | snv | 0.16 | 2 | ||
rs2391191 | 0.807 | 0.080 | 13 | 105467097 | missense variant | G/A | snv | 0.40 | 0.32 | 7 | |
rs947267 | 0.882 | 0.040 | 13 | 105487313 | intron variant | T/G | snv | 0.51 | 4 | ||
rs778294 | 0.851 | 0.040 | 13 | 105489886 | synonymous variant | C/A;T | snv | 0.27; 4.0E-06 | 0.26 | 5 | |
rs778293 | 0.807 | 0.120 | 13 | 105516850 | intergenic variant | C/A;T | snv | 7 | |||
rs1421292 | 0.925 | 0.040 | 13 | 105545886 | intergenic variant | T/A | snv | 0.39 | 3 | ||
rs4996815 | 13 | 105999312 | intron variant | G/T | snv | 0.61 | 2 | ||||
rs2018368 | 11 | 10718819 | intergenic variant | C/G | snv | 0.59 | 2 | ||||
rs17069122 | 6 | 108002555 | downstream gene variant | G/A | snv | 1.9E-02 | 2 | ||||
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 116 | |
rs1800497 | 0.620 | 0.400 | 11 | 113400106 | missense variant | G/A | snv | 0.26 | 0.26 | 56 | |
rs6277 | 0.689 | 0.480 | 11 | 113412737 | synonymous variant | G/A | snv | 0.41 | 0.38 | 36 | |
rs1801028 | 0.716 | 0.200 | 11 | 113412762 | missense variant | G/C | snv | 2.7E-02 | 1.8E-02 | 24 | |
rs1076560 | 0.776 | 0.120 | 11 | 113412966 | intron variant | C/A | snv | 0.16 | 11 | ||
rs4436578 | 0.925 | 0.080 | 11 | 113436043 | intron variant | C/T | snv | 0.73 | 4 |