Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11931074 | 0.851 | 0.080 | 4 | 89718364 | intron variant | G/A;C;T | snv | 7 | |||
rs63750802 | 0.851 | 0.080 | 14 | 73219144 | missense variant | T/G | snv | 7 | |||
rs63751032 | 0.851 | 0.080 | 14 | 73219156 | missense variant | T/A;G | snv | 7 | |||
rs63751037 | 0.790 | 0.080 | 14 | 73173642 | missense variant | A/G | snv | 7 | |||
rs193922916 | 0.827 | 0.080 | 21 | 25897619 | missense variant | G/A;C | snv | 6 | |||
rs201106962 | 0.851 | 0.080 | 4 | 89828156 | missense variant | A/C | snv | 8.0E-05 | 7.0E-05 | 5 | |
rs2306604 | 0.827 | 0.080 | 10 | 58388932 | intron variant | A/C;G;T | snv | 5 | |||
rs28936380 | 0.827 | 0.080 | 1 | 226885546 | missense variant | C/G;T | snv | 1.2E-05 | 5 | ||
rs63749835 | 0.851 | 0.080 | 14 | 73192799 | missense variant | T/C | snv | 5 | |||
rs1801474 | 0.851 | 0.080 | 6 | 162201165 | missense variant | C/T | snv | 7.1E-02 | 5.3E-02 | 4 | |
rs2281983 | 0.851 | 0.080 | 10 | 102231624 | missense variant | G/A;C;T | snv | 0.62; 8.3E-06 | 4 | ||
rs571825723 | 0.925 | 0.080 | 14 | 73211867 | missense variant | C/T | snv | 4.4E-05 | 2.8E-05 | 4 | |
rs6332 | 0.851 | 0.080 | 12 | 5494466 | synonymous variant | G/A;T | snv | 0.49; 3.2E-05 | 4 | ||
rs6347 | 0.851 | 0.080 | 5 | 1411297 | synonymous variant | T/C | snv | 0.23 | 0.32 | 4 | |
rs63750004 | 0.851 | 0.080 | 14 | 73173655 | missense variant | T/A;C | snv | 4 | |||
rs763872192 | 0.882 | 0.080 | 7 | 80672000 | missense variant | C/T | snv | 2.8E-05 | 4 | ||
rs9331896 | 0.851 | 0.080 | 8 | 27610169 | intron variant | C/G;T | snv | 4 | |||
rs9357347 | 0.851 | 0.080 | 6 | 41182853 | intergenic variant | A/C;T | snv | 4 | |||
rs1010159 | 0.882 | 0.080 | 11 | 121612692 | non coding transcript exon variant | C/T | snv | 0.55 | 0.55 | 3 | |
rs1043202 | 0.882 | 0.080 | 12 | 54182178 | missense variant | T/A | snv | 3 | |||
rs1341026713 | 0.925 | 0.080 | 21 | 25955719 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 3 | |
rs142690225 | 0.925 | 0.080 | 1 | 226894111 | missense variant | G/A | snv | 1.1E-04 | 1.1E-04 | 3 | |
rs2420616 | 0.882 | 0.080 | 10 | 119316984 | intron variant | A/G | snv | 0.69 | 3 | ||
rs2618516 | 0.882 | 0.080 | 11 | 14000092 | intron variant | T/C | snv | 0.65 | 3 | ||
rs4752293 | 0.882 | 0.080 | 10 | 119342186 | intron variant | C/T | snv | 0.74 | 3 |