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 | 4 | 162140692 | intron variant | T/C | snv | 0.53 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.080 | 4 | 161890417 | intron variant | C/T | snv | 4.7E-02 |
|
Chemically-Induced Disorders; Mental Disorders | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.080 | 4 | 161890417 | intron variant | C/T | snv | 4.7E-02 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.080 | 4 | 161890417 | intron variant | C/T | snv | 4.7E-02 |
|
Chemically-Induced Disorders; Mental Disorders | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
4 | 162117712 | intron variant | C/A | snv | 0.20 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.040 | 4 | 162145762 | intron variant | G/C | snv | 0.50 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.080 | 4 | 161903214 | intron variant | G/T | snv | 4.7E-02 |
|
Chemically-Induced Disorders; Mental Disorders | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.080 | 4 | 161903214 | intron variant | G/T | snv | 4.7E-02 |
|
Chemically-Induced Disorders | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.080 | 4 | 161903214 | intron variant | G/T | snv | 4.7E-02 |
|
Chemically-Induced Disorders; Mental Disorders | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 4 | 161420812 | intron variant | T/C | snv | 1.3E-03 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1.000 | 0.080 | 4 | 161468122 | intron variant | A/T | snv | 1.6E-02 |
|
Nervous System Diseases; Mental Disorders | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||||
|
1.000 | 0.040 | 4 | 162141456 | intron variant | C/A | snv | 0.14 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 4 | 162141605 | intron variant | A/T | snv | 0.76 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
4 | 162125024 | intron variant | G/A | snv | 0.14 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
4 | 161403710 | intron variant | G/A | snv | 0.27 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1.000 | 0.080 | 4 | 161920539 | missense variant | G/T | snv |
|
Digestive System Diseases; Neoplasms | 0.700 | 0 |