Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113681054 | 1.000 | 0.040 | 12 | 21250045 | intergenic variant | T/C | snv | 0.18 | 1 | ||
rs140104968 | 1.000 | 0.040 | 7 | 99946004 | intron variant | C/T | snv | 1.5E-02 | 1 | ||
rs140607780 | 1.000 | 0.040 | 7 | 100505900 | upstream gene variant | G/A | snv | 1.0E-02 | 1 | ||
rs62471956 | 1.000 | 0.040 | 7 | 99823462 | upstream gene variant | G/A | snv | 3.4E-02 | 1 | ||
rs147642358 | 1.000 | 0.040 | 7 | 99335136 | intron variant | G/A;T | snv | 1 | |||
rs117038461 | 1.000 | 0.040 | 7 | 100243731 | intron variant | C/T | snv | 1.5E-02 | 1 | ||
rs188845491 | 1.000 | 0.040 | 7 | 99689016 | intron variant | C/T | snv | 2.5E-04 | 1 | ||
rs1235324522 | 1.000 | 0.040 | 5 | 76732662 | missense variant | C/T | snv | 4.0E-06 | 1.4E-05 | 1 | |
rs747112750 | 1.000 | 0.040 | 1 | 202307363 | synonymous variant | C/T | snv | 4.0E-06 | 1 | ||
rs1776964 | 1.000 | 0.040 | 20 | 4899662 | synonymous variant | G/A | snv | 0.47 | 0.45 | 1 | |
rs6139591 | 1.000 | 0.040 | 20 | 4970713 | intron variant | G/A | snv | 0.40 | 1 | ||
rs61361928 | 1.000 | 0.040 | 4 | 69096657 | missense variant | T/C | snv | 2.6E-03 | 2.8E-03 | 1 | |
rs12290663 | 0.925 | 0.040 | 11 | 26141193 | intergenic variant | G/A | snv | 5.7E-02 | 2 | ||
rs144972973 | 0.925 | 0.040 | 15 | 44272494 | intergenic variant | A/G | snv | 1.8E-02 | 2 | ||
rs149232047 | 0.925 | 0.040 | 6 | 126276990 | intergenic variant | A/G | snv | 1.5E-04 | 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 | ||
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 | |||
rs62568141 | 0.925 | 0.040 | 9 | 77012344 | regulatory region variant | C/T | snv | 2.4E-02 | 2 | ||
rs9295128 | 0.925 | 0.040 | 6 | 160330499 | intergenic variant | G/T | snv | 1.1E-02 | 2 | ||
rs559110055 | 0.925 | 0.160 | 9 | 104840491 | missense variant | A/G | snv | 4.0E-06 | 2 | ||
rs147204125 | 0.925 | 0.040 | 14 | 73609035 | intron variant | A/G | snv | 9.8E-03 | 2 | ||
rs11915606 | 0.925 | 0.040 | 3 | 15633655 | intron variant | T/G | snv | 3.4E-02 | 2 | ||
rs35610040 | 1.000 | 0.040 | 20 | 23635832 | intron variant | T/C | snv | 0.19 | 2 |