Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs780759537 | 1.000 | 0.080 | 16 | 68822082 | missense variant | G/A | snv | 1.6E-05 | 4.2E-05 | 1 | |
rs747093473 | 1.000 | 0.080 | 13 | 27968819 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
rs768678989 | 1.000 | 0.080 | 7 | 116771932 | missense variant | C/T | snv | 2.8E-05 | 1 | ||
rs771333219 | 1.000 | 0.080 | 7 | 116759444 | missense variant | C/T | snv | 1.2E-04 | 8.4E-05 | 1 | |
rs63749803 | 1.000 | 0.080 | 3 | 37004421 | missense variant | T/C;G | snv | 1 | |||
rs63750297 | 1.000 | 0.080 | 3 | 37004412 | missense variant | C/A;G;T | snv | 8.0E-06 | 1 | ||
rs63751047 | 1.000 | 0.080 | 3 | 37048525 | missense variant | C/A;G | snv | 1 | |||
rs63750795 | 1.000 | 0.080 | 2 | 47480854 | missense variant | T/G | snv | 1 | |||
rs63750966 | 1.000 | 0.080 | 2 | 47403240 | missense variant | G/A;C;T | snv | 1 | |||
rs63751400 | 1.000 | 0.080 | 2 | 47480839 | missense variant | C/G;T | snv | 4.0E-06 | 1 | ||
rs1371429276 | 1.000 | 0.080 | 20 | 42472359 | missense variant | G/A | snv | 1.4E-05 | 1 | ||
rs11040869 | 0.925 | 0.080 | 11 | 1263382 | downstream gene variant | G/A | snv | 1.8E-02 | 2 | ||
rs11088680 | 0.925 | 0.080 | 21 | 13514758 | upstream gene variant | A/G | snv | 0.30 | 2 | ||
rs1887427 | 0.925 | 0.080 | 9 | 4979730 | upstream gene variant | A/G | snv | 0.21 | 2 | ||
rs1892901 | 0.925 | 0.080 | 11 | 65903422 | upstream gene variant | G/A | snv | 9.5E-03 | 2 | ||
rs26160 | 0.925 | 0.080 | 5 | 145353893 | intron variant | T/C | snv | 4.5E-03 | 2 | ||
rs36012910 | 0.925 | 0.080 | 2 | 25345310 | upstream gene variant | A/C;G | snv | 2 | |||
rs4145643 | 0.925 | 0.080 | 10 | 60803097 | regulatory region variant | G/C;T | snv | 2 | |||
rs283411 | 0.925 | 0.080 | 4 | 99344800 | intron variant | C/A;T | snv | 2 | |||
rs16941667 | 0.925 | 0.080 | 12 | 111806609 | intron variant | C/T | snv | 8.6E-02 | 2 | ||
rs1279599 | 0.925 | 0.080 | 6 | 110879025 | intron variant | G/A | snv | 0.87 | 2 | ||
rs7768897 | 0.925 | 0.080 | 6 | 110891080 | non coding transcript exon variant | A/G;T | snv | 2 | |||
rs2279284 | 0.925 | 0.080 | 11 | 13277203 | intron variant | C/T | snv | 0.25 | 2 | ||
rs911160 | 0.925 | 0.080 | 20 | 56382507 | intron variant | G/A;C | snv | 2 | |||
rs2241909 | 0.925 | 0.080 | 17 | 8205021 | synonymous variant | G/A | snv | 0.66 | 0.64 | 2 |