Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12740374 | 0.851 | 0.040 | 1 | 109274968 | 3 prime UTR variant | G/T | snv | 0.22 | 16 | ||
rs147233090 | 0.925 | 0.040 | 15 | 43735849 | intron variant | C/T | snv | 1.7E-02 | 6 | ||
rs186696265 | 0.882 | 0.040 | 6 | 160690668 | intergenic variant | C/T | snv | 1.0E-02 | 6 | ||
rs11057830 | 0.851 | 0.040 | 12 | 124822507 | intron variant | G/A | snv | 0.15 | 5 | ||
rs10757279 | 0.925 | 0.040 | 9 | 22124631 | intron variant | A/G | snv | 0.40 | 3 | ||
rs1129293 | 0.882 | 0.040 | 7 | 106872566 | synonymous variant | C/T | snv | 0.32 | 0.26 | 3 | |
rs17398575 | 0.882 | 0.040 | 7 | 106769006 | intron variant | G/A | snv | 0.20 | 3 | ||
rs181937009 | 0.925 | 0.040 | 6 | 140064258 | intron variant | A/G | snv | 0.23 | 3 | ||
rs11638352 | 0.925 | 0.040 | 15 | 44000939 | intron variant | C/A;G | snv | 2 | |||
rs11915606 | 0.925 | 0.040 | 3 | 15633655 | intron variant | T/G | snv | 3.4E-02 | 2 | ||
rs12290663 | 0.925 | 0.040 | 11 | 26141193 | intergenic variant | G/A | snv | 5.7E-02 | 2 | ||
rs138741635 | 0.925 | 0.040 | 3 | 60942161 | intron variant | T/A;G | snv | 2 | |||
rs144610116 | 0.925 | 0.040 | 4 | 38941227 | intron variant | T/C | snv | 8.6E-03 | 2 | ||
rs144972973 | 0.925 | 0.040 | 15 | 44272494 | intergenic variant | A/G | snv | 1.8E-02 | 2 | ||
rs145044782 | 0.925 | 0.040 | 7 | 7995866 | intron variant | G/A | snv | 2.9E-02 | 2 | ||
rs147204125 | 0.925 | 0.040 | 14 | 73609035 | intron variant | A/G | snv | 9.8E-03 | 2 | ||
rs148121703 | 0.925 | 0.040 | 4 | 47371654 | intron variant | TGT/- | delins | 2.6E-03 | 2 | ||
rs149232047 | 0.925 | 0.040 | 6 | 126276990 | intergenic variant | A/G | snv | 1.5E-04 | 2 | ||
rs151269874 | 0.925 | 0.040 | 16 | 75549741 | intron variant | C/T | snv | 6.2E-03 | 2 | ||
rs16985615 | 1.000 | 0.040 | 20 | 23661790 | intron variant | T/A;C | snv | 2 | |||
rs16999497 | 0.925 | 0.040 | X | 129601222 | regulatory region variant | T/C | snv | 7.8E-02 | 2 | ||
rs189889864 | 0.925 | 0.040 | 9 | 104634643 | downstream gene variant | G/A | snv | 2.8E-03 | 2 | ||
rs190543502 | 0.925 | 0.040 | 15 | 43464986 | intron variant | T/A;C | snv | 2 | |||
rs192427471 | 0.925 | 0.040 | 4 | 124644124 | intergenic variant | C/T | snv | 2.4E-03 | 2 | ||
rs201394051 | 0.925 | 0.040 | 5 | 117697919 | intergenic variant | TA/-;TATA;TATATA | delins | 2 |