Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121908212 | 0.732 | 0.160 | 19 | 13303877 | missense variant | G/A | snv | 14 | |||
rs121918799 | 0.752 | 0.120 | 2 | 166015636 | missense variant | G/C | snv | 1.7E-03 | 1.6E-03 | 14 | |
rs121908225 | 0.790 | 0.120 | 19 | 13365448 | missense variant | G/A | snv | 12 | |||
rs1057520918 | 0.790 | 0.160 | 19 | 13262780 | missense variant | C/T | snv | 11 | |||
rs121908217 | 0.851 | 0.120 | 19 | 13308452 | missense variant | C/T | snv | 4.0E-06 | 9 | ||
rs746795369 | 0.827 | 0.080 | 1 | 160139969 | missense variant | C/A;T | snv | 1.2E-05; 4.0E-06 | 6 | ||
rs886037945 | 0.827 | 0.160 | 19 | 13303584 | missense variant | C/T | snv | 6 | |||
rs121908211 | 0.882 | 0.080 | 19 | 13371744 | missense variant | C/T | snv | 5 | |||
rs121908230 | 0.882 | 0.080 | 19 | 13262789 | missense variant | C/T | snv | 5 | |||
rs794727411 | 0.851 | 0.160 | 19 | 13261526 | missense variant | C/G;T | snv | 5 | |||
rs121918632 | 0.851 | 0.120 | 2 | 165996099 | missense variant | A/G | snv | 7.0E-06 | 5 | ||
rs121918628 | 0.851 | 0.080 | 2 | 165998049 | missense variant | G/T | snv | 5 | |||
rs121908214 | 0.925 | 0.080 | 19 | 13230185 | missense variant | T/G | snv | 4 | |||
rs121909324 | 0.851 | 0.160 | 19 | 13255217 | stop gained | G/A | snv | 4 | |||
rs121918616 | 0.882 | 0.080 | 1 | 160130283 | missense variant | G/A | snv | 4.0E-06 | 3 | ||
rs28933400 | 0.882 | 0.080 | 1 | 160135510 | missense variant | T/C | snv | 3 | |||
rs28933401 | 0.882 | 0.120 | 1 | 160135246 | missense variant | G/A | snv | 3 | |||
rs121909326 | 0.882 | 0.160 | 19 | 13235219 | missense variant | A/G | snv | 3 | |||
rs121918613 | 0.925 | 0.080 | 1 | 160128667 | missense variant | A/G | snv | 2 | |||
rs1553245943 | 1.000 | 0.080 | 1 | 160137001 | missense variant | G/A | snv | 2 | |||
rs121908218 | 0.925 | 0.080 | 19 | 13303576 | missense variant | G/A;C;T | snv | 2 | |||
rs121908220 | 0.925 | 0.120 | 19 | 13235685 | missense variant | G/A | snv | 2 | |||
rs121908223 | 0.925 | 0.080 | 19 | 13262823 | missense variant | T/C | snv | 2 | |||
rs121908224 | 1.000 | 0.080 | 19 | 13235262 | missense variant | C/T | snv | 2 | |||
rs1402027664 | 0.925 | 0.080 | 19 | 13312697 | missense variant | T/C | snv | 2 |