Source: UNIPROT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121908803 | 0.925 | 0.160 | 7 | 117535281 | missense variant | C/A;T | snv | 4.0E-06 | 7.0E-06 | 1 | |
rs121908752 | 0.851 | 0.160 | 7 | 117535285 | missense variant | T/G | snv | 1.9E-04 | 1.3E-04 | 2 | |
rs397508780 | 1.000 | 0.120 | 7 | 117535341 | missense variant | T/C | snv | 1 | |||
rs397508783 | 0.925 | 0.160 | 7 | 117535363 | missense variant | T/A | snv | 2.4E-05 | 7.0E-06 | 1 | |
rs191456345 | 0.925 | 0.160 | 7 | 117536576 | missense variant | A/G | snv | 1.8E-04 | 1.1E-04 | 1 | |
rs397508804 | 1.000 | 0.120 | 7 | 117536663 | missense variant | A/T | snv | 1.2E-05 | 1 | ||
rs143486492 | 1.000 | 0.120 | 7 | 117540120 | missense variant | G/A | snv | 5.7E-04 | 5.7E-04 | 1 | |
rs150691494 | 1.000 | 0.120 | 7 | 117540132 | missense variant | A/G | snv | 2.9E-04 | 1.8E-04 | 1 | |
rs397508817 | 1.000 | 0.120 | 7 | 117540150 | missense variant | G/A | snv | 1 | |||
rs121909016 | 1.000 | 0.120 | 7 | 117540163 | missense variant | C/G | snv | 1 | |||
rs397508819 | 1.000 | 0.120 | 7 | 117540170 | missense variant | G/C;T | snv | 1 | |||
rs75763344 | 0.925 | 0.160 | 7 | 117540171 | missense variant | G/A;C;T | snv | 4.0E-06 | 1 | ||
rs121909011 | 0.807 | 0.160 | 7 | 117540230 | missense variant | C/T | snv | 5.6E-05 | 9.1E-05 | 2 | |
rs397508139 | 0.882 | 0.160 | 7 | 117540237 | missense variant | T/A;C | snv | 4.0E-06; 4.0E-06 | 1 | ||
rs77409459 | 0.851 | 0.160 | 7 | 117540243 | missense variant | C/T | snv | 2.8E-05 | 1.4E-05 | 1 | |
rs397508146 | 1.000 | 0.120 | 7 | 117540267 | missense variant | T/C | snv | 1 | |||
rs77932196 | 0.790 | 0.280 | 7 | 117540270 | missense variant | G/A;C;T | snv | 2.4E-05; 2.4E-05 | 1 | ||
rs121908753 | 0.851 | 0.160 | 7 | 117540285 | missense variant | G/A | snv | 2.4E-05 | 1 | ||
rs76879328 | 1.000 | 0.120 | 7 | 117540305 | missense variant | C/A | snv | 1 | |||
rs147422190 | 0.925 | 0.160 | 7 | 117548758 | missense variant | G/T | snv | 2.6E-04 | 3.3E-04 | 1 | |
rs74551128 | 0.807 | 0.160 | 7 | 117548795 | missense variant | C/A;T | snv | 5.3E-05; 5.7E-05 | 1 | ||
rs397508195 | 1.000 | 0.120 | 7 | 117548797 | missense variant | G/C;T | snv | 1 | |||
rs121909009 | 1.000 | 0.120 | 7 | 117548804 | missense variant | G/T | snv | 1 | |||
rs79282516 | 0.851 | 0.160 | 7 | 117559509 | missense variant | G/A;T | snv | 1 | |||
rs121909017 | 0.851 | 0.160 | 7 | 117559546 | missense variant | C/T | snv | 8.0E-06 | 1 |