Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1183194405 | 0.716 | 0.440 | 11 | 46719773 | missense variant | G/A;T | snv | 4.5E-06; 4.5E-06 | 19 | ||
rs1188383936 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 102 | ||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs121908686 | 0.882 | 0.120 | 22 | 38112558 | missense variant | C/T | snv | 9.0E-05 | 6 | ||
rs121918474 | 0.763 | 0.320 | 3 | 93905799 | missense variant | T/C | snv | 2.8E-05 | 1.4E-05 | 11 | |
rs1255283120 | 0.807 | 0.160 | 1 | 11792345 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 7 | |
rs1312546120 | 0.807 | 0.160 | 1 | 169541191 | missense variant | T/C | snv | 4.0E-06 | 7 | ||
rs13306190 | 0.807 | 0.320 | 2 | 21032408 | missense variant | G/A;C;T | snv | 1.7E-04; 8.0E-06 | 7 | ||
rs1369837875 | 0.882 | 0.200 | 22 | 38128276 | synonymous variant | G/A | snv | 4 | |||
rs1371086615 | 0.851 | 0.120 | 5 | 112828890 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 4 | |
rs141012637 | 0.851 | 0.320 | 18 | 63901881 | stop gained | C/A;T | snv | 7.0E-05 | 4 | ||
rs1431515214 | 0.925 | 0.080 | 5 | 112839790 | missense variant | G/A | snv | 4.0E-06 | 2 | ||
rs144246695 | 0.851 | 0.160 | 4 | 83310887 | missense variant | G/A | snv | 8.0E-06 | 4 | ||
rs1482856709 | 0.925 | 0.080 | 3 | 93900887 | missense variant | G/A | snv | 3 | |||
rs1799889 | 0.649 | 0.600 | 7 | 101126430 | upstream gene variant | A/G | snv | 31 | |||
rs1799963 | 0.695 | 0.400 | 11 | 46739505 | 3 prime UTR variant | G/A | snv | 9.6E-03 | 25 | ||
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 | |
rs1801131 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 93 | |
rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 174 | |
rs2066865 | 0.807 | 0.240 | 4 | 154604124 | downstream gene variant | G/A | snv | 0.26 | 10 | ||
rs268 | 0.637 | 0.480 | 8 | 19956018 | missense variant | A/G | snv | 1.3E-02 | 1.3E-02 | 41 | |
rs368927897 | 0.790 | 0.240 | 9 | 5072541 | missense variant | G/A;T | snv | 2.8E-05; 6.4E-05 | 9 | ||
rs370975770 | 1.000 | 0.080 | 22 | 38115666 | missense variant | C/T | snv | 8.9E-06 | 2.8E-05 | 1 | |
rs3789683 | 0.925 | 0.200 | 1 | 94530506 | missense variant | C/T | snv | 6.5E-03 | 1.0E-02 | 3 | |
rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 |