SVEP1, sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1, 79987
N. diseases: 21; N. variants: 15
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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
9 | 110368883 | intron variant | T/G | snv | 8.7E-02 |
|
0.800 | 1.000 | 1 | 2010 | 2010 | ||||||||||
|
1.000 | 0.040 | 9 | 110407495 | missense variant | T/C | snv | 2.6E-02 | 2.3E-02 |
|
Cardiovascular Diseases | 0.700 | 1.000 | 2 | 2017 | 2018 | ||||||
|
9 | 110392967 | intron variant | T/G | snv | 0.15 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.040 | 9 | 110569988 | intron variant | C/T | snv | 1.8E-02 |
|
Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
9 | 110576455 | intron variant | A/C | snv | 9.8E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.040 | 9 | 110407495 | missense variant | T/C | snv | 2.6E-02 | 2.3E-02 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
1.000 | 0.040 | 9 | 110407495 | missense variant | T/C | snv | 2.6E-02 | 2.3E-02 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
9 | 110385680 | intron variant | -/TGAATCCTAGTCAG | delins | 6.7E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
9 | 110408982 | intron variant | G/A;T | snv | 0.19 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
9 | 110538555 | intron variant | C/T | snv | 0.69 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
9 | 110436611 | intron variant | A/C | snv | 4.9E-02 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
9 | 110436611 | intron variant | A/C | snv | 4.9E-02 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
9 | 110549951 | missense variant | G/C;T | snv | 2.6E-02 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
9 | 110549951 | missense variant | G/C;T | snv | 2.6E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
9 | 110487920 | intron variant | G/T | snv | 2.3E-02 |
|
Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
9 | 110514390 | intron variant | G/A | snv | 0.18 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
9 | 110391049 | intron variant | T/C | snv | 0.15 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
9 | 110498428 | intron variant | T/C | snv | 2.0E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1.000 | 0.040 | 9 | 110434983 | intron variant | T/C | snv | 0.64 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2016 | 2016 |