IL18RAP, interleukin 18 receptor accessory protein, 8807
N. diseases: 41; N. variants: 22
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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.882 | 0.280 | 2 | 102437989 | intron variant | G/A | snv | 0.78 |
|
Digestive System Diseases | 0.810 | 1.000 | 2 | 2010 | 2015 | |||||||
|
2 | 102433930 | intron variant | C/T | snv | 0.22 |
|
Immune System Diseases | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
2 | 102437960 | intron variant | T/C | snv | 0.24 |
|
Immune System Diseases | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
1.000 | 0.080 | 2 | 102434684 | non coding transcript exon variant | A/G | snv | 0.22 |
|
Skin and Connective Tissue Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
2 | 102425941 | intron variant | A/G | snv | 1.8E-02 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
2 | 102444358 | intron variant | C/G | snv | 1.8E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
0.851 | 0.200 | 2 | 102418584 | upstream gene variant | A/G | snv | 0.78 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
2 | 102438960 | non coding transcript exon variant | G/A | snv | 0.26 |
|
Immune System Diseases | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
2 | 102440791 | intron variant | G/T | snv | 0.22 |
|
Immune System Diseases | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
1.000 | 0.080 | 2 | 102423413 | intron variant | C/G | snv | 0.22 |
|
Immune System Diseases | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
2 | 102419008 | intron variant | C/T | snv | 0.22 |
|
Immune System Diseases | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
1.000 | 0.080 | 2 | 102432614 | intron variant | A/G | snv | 0.55 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2010 | 2010 | |||||||
|
2 | 102435015 | non coding transcript exon variant | AA/-;A;AAA | delins |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||||
|
2 | 102435015 | non coding transcript exon variant | AA/-;A;AAA | delins |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||||
|
1.000 | 0.080 | 2 | 102426252 | intron variant | G/A | snv | 0.55 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2010 | 2010 | |||||||
|
2 | 102420217 | intron variant | C/A;T | snv |
|
Immune System Diseases | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||||
|
1.000 | 0.040 | 2 | 102446909 | intron variant | G/A | snv | 0.78 |
|
Digestive System Diseases | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||||
|
1.000 | 0.040 | 2 | 102446909 | intron variant | G/A | snv | 0.78 |
|
Digestive System Diseases | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||||
|
2 | 102424707 | intron variant | T/C | snv | 0.27 |
|
Immune System Diseases | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
2 | 102424485 | intron variant | G/A | snv | 0.25 |
|
Immune System Diseases | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
1.000 | 0.040 | 2 | 102441432 | intron variant | A/G | snv | 0.12 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2008 | 2008 | |||||||
|
0.851 | 0.200 | 2 | 102418584 | upstream gene variant | A/G | snv | 0.78 |
|
Musculoskeletal Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.851 | 0.200 | 2 | 102418584 | upstream gene variant | A/G | snv | 0.78 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.851 | 0.200 | 2 | 102418584 | upstream gene variant | A/G | snv | 0.78 |
|
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.851 | 0.200 | 2 | 102418584 | upstream gene variant | A/G | snv | 0.78 |
|
Neoplasms; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 |