MIR6886, microRNA 6886, 102465534
N. diseases: 6; N. variants: 286
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 | 19 | 11113347 | missense variant | A/G | snv |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | |||||||||||
|
0.925 | 0.080 | 19 | 11113406 | missense variant | A/T | snv |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | |||||||||||
|
0.925 | 0.080 | 19 | 11113705 | frameshift variant | C/- | del |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 19 | 11111628 | missense variant | G/A | snv |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 19 | 11111534 | missense variant | C/T | snv |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 19 | 11111567 | stop gained | G/T | snv |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 19 | 11111583 | frameshift variant | G/- | del |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 19 | 11113510 | non coding transcript exon variant | A/G | snv |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 19 | 11113588 | missense variant | G/A | snv |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | |||||||||||
|
0.925 | 0.160 | 19 | 11113603 | missense variant | C/T | snv |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 19 | 11113632 | frameshift variant | A/- | del |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 19 | 11113706 | frameshift variant | G/- | del |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 19 | 11113742 | frameshift variant | C/- | del |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 19 | 11113743 | inframe deletion | TGG/- | delins |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | |||||||||||
|
0.882 | 0.080 | 19 | 11113307 | missense variant | C/A;T | snv | 4.0E-06; 1.6E-05 |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | ||||||||||
|
1.000 | 0.080 | 19 | 11113285 | synonymous variant | C/T | snv | 1.7E-03 | 1.4E-03 |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | |||||||||
|
0.851 | 0.120 | 19 | 11113313 | missense variant | G/A;C | snv | 8.0E-06 |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | ||||||||||
|
1.000 | 0.080 | 19 | 11111620 | synonymous variant | G/A | snv | 1.2E-04 | 5.2E-04 |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | |||||||||
|
0.851 | 0.080 | 19 | 11113534 | splice acceptor variant | G/A;C | snv |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | |||||||||||
|
0.925 | 0.080 | 19 | 11113620 | missense variant | G/A;C;T | snv | 4.0E-05 |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.080 | 19 | 11113608 | missense variant | G/A;T | snv | 2.8E-05 | 2.8E-05 |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | |||||||||
|
0.827 | 0.080 | 19 | 11113376 | missense variant | G/A;C;T | snv | 1.2E-05 |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | ||||||||||
|
0.925 | 0.080 | 19 | 11113382 | missense variant | G/A;C;T | snv | 4.0E-06 |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | ||||||||||
|
0.807 | 0.200 | 19 | 11113743 | missense variant | G/A;C;T | snv | 1.2E-05; 4.0E-06 |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | ||||||||||
|
1.000 | 0.080 | 19 | 11113679 | synonymous variant | G/A | snv | 3.2E-05 | 7.7E-05 |
|
Nutritional and Metabolic Diseases | 0.700 | 0 |