Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11020802 | 0.882 | 0.080 | 11 | 94493959 | upstream gene variant | C/A;G;T | snv | 3 | |||
rs1060503291 | 0.882 | 0.080 | 5 | 112835135 | missense variant | C/T | snv | 3 | |||
rs140920401 | 0.882 | 0.080 | X | 47563284 | missense variant | G/A | snv | 3 | |||
rs868188 | 0.882 | 0.080 | 1 | 156937323 | missense variant | T/C | snv | 0.40 | 0.33 | 3 | |
rs807185 | 0.882 | 0.080 | X | 108097488 | intron variant | A/T | snv | 3 | |||
rs11212592 | 0.882 | 0.080 | 11 | 108348120 | intron variant | A/G | snv | 0.16 | 3 | ||
rs3866958 | 0.882 | 0.080 | 17 | 19377693 | intron variant | A/C;T | snv | 0.89 | 3 | ||
rs575508709 | 0.882 | 0.080 | 6 | 31649333 | missense variant | C/G | snv | 4.0E-06 | 3 | ||
rs7501331 | 0.882 | 0.080 | 16 | 81280891 | missense variant | C/T | snv | 0.21 | 0.18 | 3 | |
rs6141383 | 0.882 | 0.080 | 20 | 33301335 | missense variant | G/A | snv | 1.7E-03 | 9.9E-04 | 3 | |
rs868021367 | 0.882 | 0.080 | 7 | 140753319 | missense variant | C/G | snv | 3 | |||
rs756402191 | 0.882 | 0.080 | 10 | 73913605 | missense variant | G/A;T | snv | 1.2E-04; 4.0E-05 | 3 | ||
rs652311 | 0.882 | 0.080 | 11 | 108369342 | intron variant | G/A | snv | 0.54 | 3 | ||
rs16832404 | 0.882 | 0.080 | 2 | 190188403 | intron variant | T/C | snv | 0.12 | 3 | ||
rs507879 | 0.882 | 0.080 | 11 | 105007200 | missense variant | T/A;C;G | snv | 0.43 | 0.49 | 3 | |
rs1410508127 | 0.882 | 0.080 | 10 | 113679831 | missense variant | A/C;G | snv | 3 | |||
rs1422012687 | 0.882 | 0.080 | 1 | 15524124 | stop gained | C/A;T | snv | 7.2E-06; 7.2E-06 | 3 | ||
rs1049337 | 0.882 | 0.080 | 7 | 116560533 | 3 prime UTR variant | C/T | snv | 0.25 | 3 | ||
rs2977549 | 0.882 | 0.080 | 8 | 133229790 | 3 prime UTR variant | C/A;T | snv | 3 | |||
rs3739262 | 0.882 | 0.080 | 8 | 133193470 | intron variant | G/A | snv | 0.24 | 3 | ||
rs754958 | 0.882 | 0.080 | 8 | 133226528 | intron variant | G/A;T | snv | 3 | |||
rs769236 | 0.882 | 0.080 | 4 | 121823883 | 5 prime UTR variant | C/A;T | snv | 3 | |||
rs2282987 | 0.882 | 0.080 | 7 | 92683489 | intron variant | G/C | snv | 3.7E-02 | 3 | ||
rs10487372 | 0.882 | 0.080 | 7 | 117560845 | intron variant | C/T | snv | 0.13 | 3 | ||
rs876659871 | 0.882 | 0.080 | 22 | 28719462 | missense variant | C/T | snv | 7.0E-06 | 3 |