Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3753584 | 0.827 | 0.080 | 1 | 11804529 | 5 prime UTR variant | T/C | snv | 0.14 | 10 | ||
rs12108497 | 0.851 | 0.080 | 4 | 184650403 | intron variant | C/G;T | snv | 6 | |||
rs1760893 | 0.807 | 0.080 | 14 | 20412501 | intron variant | C/A | snv | 0.89 | 6 | ||
rs10817938 | 0.882 | 0.080 | 9 | 97700127 | non coding transcript exon variant | T/C | snv | 3.2E-02 | 5 | ||
rs12800438 | 1.000 | 0.080 | 11 | 71459957 | non coding transcript exon variant | G/A;T | snv | 5 | |||
rs2143571 | 0.827 | 0.080 | 22 | 43995806 | intron variant | G/A | snv | 0.25 | 5 | ||
rs2299939 | 0.827 | 0.080 | 10 | 87897393 | intron variant | C/A;T | snv | 5 | |||
rs3131003 | 0.925 | 0.080 | 6 | 31125705 | 5 prime UTR variant | G/A | snv | 0.52 | 5 | ||
rs3807992 | 0.925 | 0.080 | 7 | 116557191 | intron variant | G/A | snv | 0.28 | 5 | ||
rs621559 | 0.827 | 0.080 | 1 | 43179740 | intron variant | G/A | snv | 0.18 | 5 | ||
rs9267673 | 0.925 | 0.080 | 6 | 31915902 | intron variant | C/A;T | snv | 0.12 | 5 | ||
rs1200055659 | 0.851 | 0.080 | 1 | 153614902 | missense variant | G/A | snv | 7.0E-06 | 4 | ||
rs1234220 | 0.851 | 0.080 | 10 | 87885716 | intron variant | A/G | snv | 9.1E-02 | 4 | ||
rs2069852 | 0.925 | 0.080 | 7 | 22732641 | downstream gene variant | G/A;C | snv | 4 | |||
rs2890658 | 0.925 | 0.080 | 9 | 5465130 | intron variant | C/A;T | snv | 4 | |||
rs4663402 | 0.851 | 0.080 | 2 | 233285017 | intron variant | A/T | snv | 5.1E-02 | 4 | ||
rs6588147 | 0.851 | 0.080 | 1 | 65469811 | intron variant | G/A | snv | 0.70 | 4 | ||
rs80309960 | 0.851 | 0.080 | 2 | 216122110 | missense variant | T/A | snv | 3.5E-04 | 1.1E-03 | 4 | |
rs10485505 | 1.000 | 0.080 | 20 | 34437762 | intron variant | C/G;T | snv | 3 | |||
rs10519613 | 1.000 | 0.080 | 4 | 141732931 | 3 prime UTR variant | C/A | snv | 0.10 | 3 | ||
rs10836347 | 1.000 | 0.080 | 11 | 35231586 | 3 prime UTR variant | C/T | snv | 0.11 | 3 | ||
rs11564475 | 0.882 | 0.080 | 3 | 41238542 | intron variant | A/G | snv | 3.7E-02 | 3 | ||
rs121913676 | 0.925 | 0.080 | 7 | 116783421 | missense variant | G/A;C;T | snv | 3 | |||
rs157077 | 1.000 | 0.080 | 10 | 104278136 | intron variant | T/C | snv | 0.45 | 0.53 | 3 | |
rs17006625 | 0.925 | 0.080 | 3 | 20119604 | missense variant | A/C;G | snv | 4.0E-06; 3.3E-02 | 3 |