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 | 0.120 | 10 | 6430929 | missense variant | G/C;T | snv | 4.0E-06; 0.17 |
|
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases | 0.800 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.790 | 0.160 | 10 | 6485181 | missense variant | G/A | snv | 0.31 | 0.30 |
|
Digestive System Diseases | 0.710 | 1.000 | 2 | 2016 | 2019 | ||||||
|
0.925 | 0.080 | 10 | 6579811 | intron variant | T/C | snv | 0.51 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.700 | 1.000 | 2 | 2019 | 2019 | |||||||
|
1.000 | 0.040 | 10 | 6479572 | intron variant | G/A | snv | 0.13 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
10 | 6470618 | intron variant | A/G | snv | 3.4E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
10 | 6470618 | intron variant | A/G | snv | 3.4E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
10 | 6470618 | intron variant | A/G | snv | 3.4E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
0.790 | 0.160 | 10 | 6485181 | missense variant | G/A | snv | 0.31 | 0.30 |
|
Digestive System Diseases | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
0.790 | 0.160 | 10 | 6485181 | missense variant | G/A | snv | 0.31 | 0.30 |
|
Digestive System Diseases | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
0.790 | 0.160 | 10 | 6485181 | missense variant | G/A | snv | 0.31 | 0.30 |
|
Musculoskeletal Diseases | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
0.790 | 0.160 | 10 | 6485181 | missense variant | G/A | snv | 0.31 | 0.30 |
|
Skin and Connective Tissue Diseases | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
0.790 | 0.160 | 10 | 6485181 | missense variant | G/A | snv | 0.31 | 0.30 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1.000 | 0.040 | 10 | 6480736 | intron variant | G/C | snv | 0.12 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
10 | 6564579 | intron variant | C/T | snv | 0.10 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1.000 | 0.040 | 10 | 6480946 | intron variant | T/G | snv | 0.77 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 10 | 6484535 | intron variant | T/G | snv | 0.30 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 10 | 6478587 | intron variant | A/G | snv | 0.18 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 10 | 6485382 | intron variant | A/C | snv | 0.46 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 10 | 6483991 | intron variant | G/C;T | snv |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 0.040 | 10 | 6478622 | intron variant | T/C | snv | 0.11 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.925 | 0.080 | 10 | 6579811 | intron variant | T/C | snv | 0.51 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.790 | 0.160 | 10 | 6485181 | missense variant | G/A | snv | 0.31 | 0.30 |
|
Digestive System Diseases | 0.700 | 0 |