LPA, lipoprotein(a), 4018
N. diseases: 340; N. variants: 49
Source: ALL
| Variant | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Disease Class | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 0.040 | 6 | 160584578 | intron variant | C/T | snv | 4.5E-02 |
|
0.700 | 1.000 | 2 | 2013 | 2017 | ||||||||
|
1.000 | 0.040 | 6 | 160596331 | intron variant | G/A | snv | 3.6E-02 |
|
0.700 | 1.000 | 2 | 2017 | 2019 | ||||||||
|
1.000 | 0.040 | 6 | 160597142 | intron variant | C/T | snv | 0.63 |
|
0.700 | 1.000 | 2 | 2017 | 2019 | ||||||||
|
6 | 160534681 | intron variant | G/C;T | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||||
|
6 | 160610628 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2015 | 2015 | |||||||||||
|
6 | 160608638 | intron variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||||
|
6 | 160647203 | intron variant | A/T | snv | 8.9E-03 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
6 | 160564494 | intron variant | G/A | snv | 4.3E-02 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
6 | 160661663 | intron variant | T/C | snv | 0.66 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||||
|
1.000 | 0.040 | 6 | 160591981 | intron variant | T/C | snv | 2.8E-02 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
6 | 160570969 | intron variant | C/G | snv | 2.1E-02 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
6 | 160583319 | intron variant | G/A | snv | 4.9E-03 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
6 | 160590288 | intron variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
6 | 160646897 | intron variant | T/G | snv | 8.7E-03 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
6 | 160653951 | intron variant | T/A;G | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||||
|
6 | 160577116 | intron variant | G/T | snv | 0.21 | 0.19 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | |||||||||
|
6 | 160601075 | missense variant | C/A;T | snv | 1.6E-05; 7.7E-03 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
6 | 160531784 | missense variant | T/C | snv | 1.0E-02 | 1.0E-02 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
6 | 160532610 | missense variant | A/G;T | snv | 2.1E-02; 1.2E-05 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
1.000 | 0.040 | 6 | 160585045 | splice donor variant | C/A;T | snv | 1.2E-05; 4.1E-02 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
6 | 160566028 | intron variant | A/G | snv | 9.9E-03 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
1.000 | 0.040 | 6 | 160559298 | intron variant | T/C | snv | 0.57 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
6 | 160570766 | intron variant | C/T | snv | 0.80 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
1.000 | 0.040 | 6 | 160598834 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
6 | 160565883 | intron variant | A/C | snv | 0.85 |
|
0.700 | 1.000 | 1 | 2017 | 2017 |