STARD3, StAR related lipid transfer domain containing 3, 10948
N. diseases: 21; N. variants: 7
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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.925 | 0.080 | 17 | 39657603 | intron variant | G/C | snv | 0.52 |
|
0.800 | 1.000 | 4 | 2010 | 2019 | ||||||||
|
0.925 | 0.080 | 17 | 39657603 | intron variant | G/C | snv | 0.52 |
|
0.700 | 1.000 | 2 | 2010 | 2013 | ||||||||
|
1.000 | 0.080 | 17 | 39661229 | non coding transcript exon variant | T/C | snv | 0.61 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.700 | 1.000 | 2 | 2010 | 2011 | |||||||
|
0.925 | 0.080 | 17 | 39653965 | intron variant | C/G | snv | 0.51 |
|
0.700 | 1.000 | 2 | 2018 | 2019 | ||||||||
|
0.925 | 0.080 | 17 | 39657603 | intron variant | G/C | snv | 0.52 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.925 | 0.080 | 17 | 39657603 | intron variant | G/C | snv | 0.52 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
17 | 39644735 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
0.827 | 0.280 | 17 | 39657827 | missense variant | G/A | snv | 0.62 | 0.52 |
|
Respiratory Tract Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2010 | 2010 | ||||||
|
0.827 | 0.280 | 17 | 39657827 | missense variant | G/A | snv | 0.62 | 0.52 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
|
0.827 | 0.280 | 17 | 39657827 | missense variant | G/A | snv | 0.62 | 0.52 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||||
|
0.827 | 0.280 | 17 | 39657827 | missense variant | G/A | snv | 0.62 | 0.52 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
|
0.827 | 0.280 | 17 | 39657827 | missense variant | G/A | snv | 0.62 | 0.52 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.827 | 0.280 | 17 | 39657827 | missense variant | G/A | snv | 0.62 | 0.52 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
|
1.000 | 0.080 | 17 | 39654542 | intron variant | C/G;T | snv |
|
Respiratory Tract Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.925 | 0.080 | 17 | 39653965 | intron variant | C/G | snv | 0.51 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.925 | 0.080 | 17 | 39653965 | intron variant | C/G | snv | 0.51 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.925 | 0.080 | 17 | 39653965 | intron variant | C/G | snv | 0.51 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.925 | 0.080 | 17 | 39651445 | intron variant | A/C | snv | 0.66 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.925 | 0.080 | 17 | 39651445 | intron variant | A/C | snv | 0.66 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
0.925 | 0.080 | 17 | 39651445 | intron variant | A/C | snv | 0.66 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.925 | 0.080 | 17 | 39651445 | intron variant | A/C | snv | 0.66 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 |