Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2420946 | 0.851 | 0.160 | 10 | 121591810 | intron variant | T/C | snv | 0.56 | 4 | ||
rs121917739 | 0.882 | 0.080 | 15 | 40718818 | missense variant | G/A | snv | 3.7E-04 | 1.7E-03 | 4 | |
rs34434221 | 0.882 | 0.080 | 15 | 85579644 | missense variant | A/C | snv | 2.2E-02 | 2.2E-02 | 3 | |
rs6960867 | 0.882 | 0.080 | 7 | 92083384 | missense variant | A/G | snv | 0.36 | 0.34 | 3 | |
rs113211432 | 0.882 | 0.080 | 2 | 214767532 | frameshift variant | -/TG | delins | 3 | |||
rs2070094 | 0.882 | 0.080 | 2 | 214767531 | missense variant | C/A;T | snv | 1.6E-05; 0.37 | 3 | ||
rs386654966 | 0.882 | 0.080 | 2 | 214767531 | missense variant | CA/AG;TG | mnv | 3 | |||
rs747364414 | 0.882 | 0.080 | 17 | 43082496 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 3 | |
rs80357125 | 0.882 | 0.080 | 17 | 43063940 | missense variant | C/A;G;T | snv | 3 | |||
rs886039958 | 0.882 | 0.080 | 17 | 43093956 | frameshift variant | A/-;AA | delins | 3 | |||
rs41293475 | 0.882 | 0.080 | 13 | 32332629 | missense variant | C/G;T | snv | 7.6E-04 | 3 | ||
rs4645959 | 0.882 | 0.080 | 8 | 127738294 | missense variant | A/C;G | snv | 1.6E-05; 2.3E-02 | 3 | ||
rs3112612 | 0.882 | 0.080 | 16 | 52601252 | intron variant | G/A | snv | 0.44 | 3 | ||
rs878853646 | 0.882 | 0.080 | 9 | 21971106 | missense variant | C/A;T | snv | 4.3E-06; 8.6E-06 | 3 | ||
rs28359178 | 0.882 | 0.280 | MT | 13708 | missense variant | G/A | snv | 3 | |||
rs17663555 | 1.000 | 0.080 | 5 | 73136209 | intron variant | C/A;G;T | snv | 3 | |||
rs1302297709 | 0.882 | 0.080 | 17 | 58703319 | missense variant | A/G | snv | 3 | |||
rs767915085 | 0.882 | 0.080 | 16 | 28606122 | missense variant | T/C | snv | 8.0E-06 | 7.1E-06 | 3 | |
rs398122697 | 0.925 | 0.080 | 17 | 43049170 | missense variant | A/G | snv | 4.0E-06 | 2 | ||
rs566164 | 1.000 | 0.080 | 6 | 109185258 | intron variant | A/G | snv | 0.73 | 2 | ||
rs11075884 | 1.000 | 0.080 | 16 | 71321332 | intergenic variant | A/C;G | snv | 1 | |||
rs2241268 | 1.000 | 0.080 | 15 | 85735078 | missense variant | G/A | snv | 0.22 | 0.19 | 1 | |
rs4843075 | 1.000 | 0.080 | 15 | 85581324 | missense variant | G/A;C | snv | 0.61; 4.0E-06 | 1 | ||
rs758898660 | 1.000 | 0.080 | 5 | 73892052 | missense variant | G/A | snv | 4.4E-06 | 1 | ||
rs756522395 | 1.000 | 0.080 | 11 | 108257484 | missense variant | C/G;T | snv | 1 |