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 | |
rs429358 | 0.590 | 0.600 | 19 | 44908684 | missense variant | T/C | snv | 0.14 | 0.16 | 66 | |
rs3775291 | 0.602 | 0.640 | 4 | 186082920 | missense variant | C/G;T | snv | 1.2E-04; 0.28 | 51 | ||
rs3732378 | 0.620 | 0.720 | 3 | 39265671 | missense variant | G/A | snv | 0.14 | 0.12 | 48 | |
rs3732379 | 0.637 | 0.680 | 3 | 39265765 | missense variant | C/T | snv | 0.22 | 0.22 | 38 | |
rs800292 | 0.645 | 0.560 | 1 | 196673103 | missense variant | G/A | snv | 0.32 | 0.40 | 33 | |
rs1130864 | 0.672 | 0.520 | 1 | 159713301 | 3 prime UTR variant | G/A | snv | 0.26 | 27 | ||
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 | |
rs2070895 | 0.807 | 0.120 | 15 | 58431740 | intron variant | G/A | snv | 0.33 | 15 | ||
rs11200638 | 0.724 | 0.280 | 10 | 122461028 | non coding transcript exon variant | G/A | snv | 0.23 | 14 | ||
rs61755783 | 0.763 | 0.080 | 6 | 42721911 | missense variant | G/A | snv | 1.4E-05 | 11 | ||
rs2230199 | 0.763 | 0.240 | 19 | 6718376 | missense variant | G/C;T | snv | 0.15 | 10 | ||
rs17231506 | 0.851 | 0.040 | 16 | 56960616 | upstream gene variant | C/G;T | snv | 0.28 | 10 | ||
rs9332739 | 0.763 | 0.360 | 6 | 31936027 | missense variant | G/A;C | snv | 4.1E-06; 3.9E-02 | 10 | ||
rs61755792 | 0.763 | 0.160 | 6 | 42721821 | missense variant | G/A;C | snv | 10 | |||
rs2740488 | 0.827 | 0.120 | 9 | 104899461 | intron variant | A/C | snv | 0.29 | 9 | ||
rs2043085 | 0.827 | 0.080 | 15 | 58388755 | intron variant | T/C | snv | 0.54 | 9 | ||
rs4151667 | 0.790 | 0.320 | 6 | 31946247 | missense variant | T/A | snv | 3.9E-02 | 3.4E-02 | 9 | |
rs10737680 | 0.827 | 0.080 | 1 | 196710325 | intron variant | A/C | snv | 0.44 | 9 | ||
rs641153 | 0.790 | 0.160 | 6 | 31946403 | missense variant | G/A;T | snv | 9.6E-02; 4.1E-06 | 7 | ||
rs10033900 | 0.807 | 0.040 | 4 | 109737911 | intron variant | T/C | snv | 0.54 | 7 | ||
rs147859257 | 0.827 | 0.040 | 19 | 6718135 | missense variant | T/G | snv | 2.8E-03 | 2.4E-03 | 6 | |
rs10922109 | 0.827 | 0.080 | 1 | 196735502 | intron variant | C/A | snv | 0.46 | 6 | ||
rs570618 | 0.827 | 0.040 | 1 | 196687934 | intron variant | T/G | snv | 0.69 | 6 |