Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11887534 | 0.653 | 0.440 | 2 | 43839108 | missense variant | G/A;C | snv | 6.4E-06; 6.7E-02 | 29 | ||
rs2287622 | 0.724 | 0.240 | 2 | 168973818 | missense variant | A/C;G;T | snv | 0.57 | 16 | ||
rs1382897404 | 0.851 | 0.040 | 2 | 169018071 | missense variant | C/G | snv | 7.0E-06 | 4 | ||
rs1051861187 | 0.827 | 0.080 | 7 | 87409385 | missense variant | A/G | snv | 6 | |||
rs72552778 | 0.827 | 0.040 | 7 | 87447080 | missense variant | G/A | snv | 1.6E-04 | 1.7E-04 | 5 | |
rs375315619 | 0.851 | 0.080 | 7 | 87440230 | missense variant | T/C | snv | 2.0E-04 | 9.8E-05 | 4 | |
rs45575636 | 0.882 | 0.080 | 7 | 87431528 | missense variant | C/G;T | snv | 4.0E-06; 4.5E-03 | 3 | ||
rs66904256 | 0.882 | 0.080 | 7 | 87439777 | missense variant | T/A | snv | 3 | |||
rs1257887155 | 0.925 | 0.040 | 7 | 87440228 | missense variant | C/T | snv | 7.0E-06 | 2 | ||
rs387906528 | 0.925 | 0.040 | 7 | 87443346 | frameshift variant | CT/TTG | delins | 2 | |||
rs765478923 | 0.925 | 0.040 | 7 | 87447182 | missense variant | G/A | snv | 1.6E-05 | 2.8E-05 | 2 | |
rs8187788 | 0.925 | 0.040 | 7 | 87462827 | missense variant | G/C | snv | 7.2E-04 | 7.3E-04 | 2 | |
rs121918442 | 1.000 | 0.040 | 7 | 87406293 | missense variant | G/A;T | snv | 2.4E-05 | 1 | ||
rs1262922848 | 1.000 | 0.040 | 7 | 87408066 | missense variant | G/A | snv | 1 | |||
rs1408217402 | 1.000 | 0.040 | 7 | 87454583 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
rs1411970557 | 1.000 | 0.040 | 7 | 87462811 | missense variant | A/C | snv | 4.0E-06 | 7.0E-06 | 1 | |
rs141677867 | 1.000 | 0.040 | 7 | 87423940 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 1 | |
rs142794414 | 1.000 | 0.040 | 7 | 87472655 | missense variant | G/A;T | snv | 4.8E-04; 8.0E-06; 4.0E-06 | 1.2E-03 | 1 | |
rs372685632 | 1.000 | 0.040 | 7 | 87462904 | missense variant | C/T | snv | 8.8E-05 | 6.3E-05 | 1 | |
rs397514620 | 1.000 | 0.040 | 7 | 87439765 | missense variant | G/A;C | snv | 8.0E-06 | 1 | ||
rs571555115 | 1.000 | 0.040 | 7 | 87431519 | missense variant | G/A | snv | 3.2E-05 | 2.8E-05 | 1 | |
rs72552776 | 1.000 | 0.040 | 7 | 87431525 | missense variant | A/T | snv | 4.0E-06 | 1 | ||
rs72552779 | 1.000 | 0.040 | 7 | 87447137 | missense variant | A/G | snv | 1 | |||
rs759787957 | 1.000 | 0.040 | 7 | 87411894 | missense variant | G/C | snv | 4.0E-06 | 1 | ||
rs761238221 | 1.000 | 0.040 | 7 | 87439752 | missense variant | C/A;T | snv | 8.0E-06; 3.6E-05 | 1 |