Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11554273 | 0.689 | 0.240 | 20 | 58909365 | missense variant | C/A;G;T | snv | 4.0E-06 | 22 | ||
rs56149945 | 0.595 | 0.680 | 5 | 143399752 | missense variant | T/A;C | snv | 2.0E-02 | 49 | ||
rs41423247 | 0.695 | 0.440 | 5 | 143399010 | intron variant | G/C | snv | 0.31 | 23 | ||
rs6198 | 0.724 | 0.480 | 5 | 143278056 | 3 prime UTR variant | T/C | snv | 0.12 | 16 | ||
rs6189 | 0.827 | 0.240 | 5 | 143400774 | missense variant | C/A;T | snv | 4.0E-06; 1.8E-02 | 6 | ||
rs6190 | 0.827 | 0.120 | 5 | 143400772 | missense variant | C/G;T | snv | 4.0E-06; 1.8E-02 | 6 | ||
rs1333998849 | 0.925 | 0.040 | 5 | 143295540 | missense variant | T/C | snv | 1.4E-05 | 2 | ||
rs76308115 | 0.851 | 0.080 | 2 | 178014454 | stop gained | G/A | snv | 2.9E-03 | 2.9E-03 | 5 | |
rs386352352 | 0.851 | 0.080 | 19 | 14097604 | missense variant | A/C | snv | 6 |