Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs137854619 | 0.925 | 0.120 | 3 | 38550917 | missense variant | C/T | snv | 2.7E-04 | 7.7E-05 | 1 | |
rs137854614 | 0.882 | 0.120 | 3 | 38550988 | missense variant | T/C | snv | 1 | |||
rs137854615 | 0.851 | 0.120 | 3 | 38550989 | missense variant | A/G | snv | 1 | |||
rs727504495 | 1.000 | 0.080 | 3 | 38550998 | missense variant | C/A;T | snv | 4.0E-06; 2.0E-05 | 1 | ||
rs199473317 | 0.882 | 0.120 | 3 | 38551003 | missense variant | T/C | snv | 1 | |||
rs137854601 | 0.776 | 0.120 | 3 | 38551022 | stop gained | C/A;T | snv | 4.0E-06 | 2 | ||
rs199473634 | 0.925 | 0.120 | 3 | 38551036 | missense variant | G/A | snv | 4.0E-05 | 7.7E-05 | 2 | |
rs199473314 | 1.000 | 0.120 | 3 | 38551043 | missense variant | C/T | snv | 1.6E-05 | 2.1E-05 | 1 | |
rs199473311 | 0.882 | 0.120 | 3 | 38551070 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
rs199473632 | 1.000 | 0.120 | 3 | 38551072 | missense variant | T/C | snv | 1 | |||
rs199473310 | 1.000 | 0.120 | 3 | 38551076 | missense variant | T/A;C;G | snv | 1 | |||
rs199473309 | 1.000 | 0.080 | 3 | 38551082 | missense variant | C/A | snv | 1 | |||
rs199473631 | 0.925 | 0.120 | 3 | 38551085 | missense variant | C/T | snv | 1 | |||
rs199473308 | 1.000 | 0.120 | 3 | 38551090 | missense variant | A/T | snv | 1 | |||
rs199473307 | 1.000 | 0.120 | 3 | 38551091 | missense variant | G/A | snv | 1 | |||
rs199473629 | 1.000 | 0.080 | 3 | 38551144 | missense variant | C/T | snv | 1 | |||
rs199473305 | 0.925 | 0.080 | 3 | 38551145 | missense variant | C/T | snv | 1.4E-05 | 1 | ||
rs199473304 | 1.000 | 0.080 | 3 | 38551154 | missense variant | C/T | snv | 1 | |||
rs199473303 | 0.925 | 0.120 | 3 | 38551157 | missense variant | G/A;T | snv | 3.6E-05; 4.0E-06 | 1 | ||
rs193922726 | 1.000 | 0.080 | 3 | 38551188 | missense variant | G/A;C | snv | 6.0E-05 | 1 | ||
rs199473302 | 1.000 | 0.080 | 3 | 38551190 | missense variant | A/G | snv | 1 | |||
rs199473300 | 1.000 | 0.120 | 3 | 38551204 | missense variant | G/T | snv | 1.4E-05 | 1 | ||
rs199473299 | 1.000 | 0.080 | 3 | 38551208 | missense variant | T/C | snv | 1 | |||
rs199473628 | 1.000 | 0.080 | 3 | 38551231 | missense variant | T/C | snv | 1 | |||
rs199473298 | 1.000 | 0.080 | 3 | 38551238 | missense variant | C/T | snv | 4.0E-06 | 1 |