Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs267607144 | 0.716 | 0.360 | 12 | 109800665 | missense variant | C/T | snv | 17 | |||
rs80356814 | 0.732 | 0.320 | 1 | 156138697 | synonymous variant | C/T | snv | 8.0E-06 | 15 | ||
rs121913603 | 0.732 | 0.160 | 1 | 161306722 | missense variant | T/C;G | snv | 2.0E-05 | 12 | ||
rs121913595 | 0.742 | 0.160 | 1 | 161306785 | missense variant | G/A;T | snv | 11 | |||
rs137852973 | 0.752 | 0.200 | 11 | 62702493 | missense variant | G/A;C | snv | 7.0E-06 | 13 | ||
rs121918312 | 0.776 | 0.160 | 10 | 119672373 | missense variant | C/A;T | snv | 11 | |||
rs28940291 | 0.776 | 0.080 | 1 | 11992660 | missense variant | G/A | snv | 4.0E-06 | 9 | ||
rs58982919 | 0.790 | 0.080 | 8 | 24956223 | missense variant | T/C | snv | 10 | |||
rs104894080 | 0.790 | 0.120 | 8 | 74364005 | missense variant | C/T | snv | 3.2E-05 | 4.2E-05 | 9 | |
rs104894621 | 0.790 | 0.080 | 17 | 15239575 | missense variant | G/A | snv | 9 | |||
rs104894077 | 0.790 | 0.080 | 8 | 74361886 | stop gained | C/T | snv | 7.6E-05 | 1.5E-04 | 8 | |
rs119103267 | 0.790 | 0.160 | 1 | 12009641 | missense variant | C/T | snv | 2.5E-04 | 2.8E-04 | 7 | |
rs60864230 | 0.790 | 0.280 | 1 | 156130658 | missense variant | G/A;C;T | snv | 4.0E-06 | 7 | ||
rs80338933 | 0.807 | 0.080 | 5 | 149026872 | stop gained | G/A | snv | 7.5E-04; 4.0E-06 | 6.6E-04 | 9 | |
rs121918054 | 0.807 | 0.240 | 15 | 89323460 | missense variant | C/G;T | snv | 6.9E-04; 4.0E-06 | 8 | ||
rs142000963 | 0.807 | 0.240 | 1 | 156138719 | missense variant | C/A;T | snv | 1.2E-03 | 8 | ||
rs104894161 | 0.807 | 0.080 | 10 | 62813563 | missense variant | G/A | snv | 6 | |||
rs104894619 | 0.827 | 0.120 | 17 | 15231047 | missense variant | G/A | snv | 4.0E-03 | 3.7E-03 | 9 | |
rs104894351 | 0.827 | 0.080 | 12 | 119187078 | missense variant | A/C;G | snv | 7 | |||
rs1553259662 | 0.827 | 0.200 | 1 | 161306821 | missense variant | A/G | snv | 7 | |||
rs104894345 | 0.827 | 0.080 | 12 | 119187080 | missense variant | G/C;T | snv | 6 | |||
rs119103268 | 0.827 | 0.080 | 1 | 11992689 | missense variant | C/T | snv | 6 | |||
rs104894159 | 0.827 | 0.080 | 10 | 62813413 | missense variant | G/A | snv | 5 | |||
rs121913597 | 0.827 | 0.160 | 1 | 161307268 | missense variant | T/A | snv | 5 | |||
rs397515323 | 0.851 | 0.080 | X | 24503479 | missense variant | G/A | snv | 7 |