Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1061170 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 72 | |
rs10490924 | 0.716 | 0.240 | 10 | 122454932 | missense variant | G/T | snv | 0.26 | 0.23 | 16 | |
rs121913059 | 0.716 | 0.280 | 1 | 196747245 | missense variant | C/T | snv | 1.4E-04 | 1.9E-04 | 16 | |
rs11200638 | 0.724 | 0.280 | 10 | 122461028 | non coding transcript exon variant | G/A | snv | 0.23 | 14 | ||
rs641153 | 0.790 | 0.160 | 6 | 31946403 | missense variant | G/A;T | snv | 9.6E-02; 4.1E-06 | 7 | ||
rs570618 | 0.827 | 0.040 | 1 | 196687934 | intron variant | T/G | snv | 0.69 | 6 | ||
rs148060787 | 0.851 | 0.080 | 11 | 61962853 | missense variant | C/G;T | snv | 4.4E-04 | 5 | ||
rs1800995 | 0.851 | 0.080 | 11 | 61955906 | missense variant | GC/AA | mnv | 5 | |||
rs1805142 | 0.851 | 0.080 | 11 | 61955825 | stop gained | G/C;T | snv | 2.7E-05 | 5 | ||
rs281865275 | 0.851 | 0.080 | 11 | 61957397 | missense variant | C/G;T | snv | 8.0E-06; 2.8E-05 | 5 |