HSPB1, heat shock protein family B (small) member 1, 3315
N. diseases: 395; N. variants: 31
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 | 0.080 | 7 | 76303855 | missense variant | C/G | snv |
|
Nervous System Diseases | 0.800 | 1.000 | 11 | 2004 | 2017 | ||||||||
|
0.925 | 0.040 | 7 | 76303007 | missense variant | C/A | snv |
|
Nervous System Diseases | 0.800 | 1.000 | 11 | 2004 | 2017 | ||||||||
|
0.925 | 0.080 | 7 | 76304007 | missense variant | C/G;T | snv |
|
Nervous System Diseases | 0.800 | 1.000 | 11 | 2004 | 2017 | ||||||||
|
1.000 | 0.040 | 7 | 76304100 | missense variant | C/T | snv |
|
Nervous System Diseases | 0.800 | 1.000 | 11 | 2004 | 2017 | ||||||||
|
0.925 | 0.080 | 7 | 76303841 | missense variant | C/A;G;T | snv |
|
Nervous System Diseases | 0.800 | 1.000 | 11 | 2004 | 2017 | ||||||||
|
0.851 | 0.080 | 7 | 76303816 | missense variant | C/A;T | snv | 8.0E-06 |
|
Nervous System Diseases | 0.800 | 1.000 | 11 | 2004 | 2017 | |||||||
|
1.000 | 0.040 | 7 | 76302870 | missense variant | G/A | snv | 1.1E-05 |
|
Nervous System Diseases | 0.800 | 0 | ||||||||||
|
1.000 | 0.040 | 7 | 76303820 | missense variant | A/G | snv | 4.8E-05 | 2.9E-05 |
|
Nervous System Diseases | 0.800 | 0 | |||||||||
|
1.000 | 0.040 | 7 | 76304115 | stop gained | C/A;G;T | snv | 1.2E-05; 4.1E-06; 4.1E-06 |
|
Nervous System Diseases | 0.800 | 0 | ||||||||||
|
1.000 | 0.040 | 7 | 76302833 | missense variant | G/A;C | snv |
|
Nervous System Diseases | 0.700 | 1.000 | 11 | 2004 | 2017 | ||||||||
|
0.925 | 0.080 | 7 | 76302828 | missense variant | C/G;T | snv | 4.4E-06 |
|
Nervous System Diseases | 0.700 | 1.000 | 11 | 2004 | 2017 | |||||||
|
0.882 | 0.080 | 7 | 76304099 | missense variant | C/T | snv |
|
Nervous System Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.040 | 7 | 76302886 | frameshift variant | -/C | delins | 2.1E-05 |
|
Nervous System Diseases | 0.700 | 0 | ||||||||||
|
1.000 | 0.040 | 7 | 76303852 | missense variant | A/G | snv |
|
Nervous System Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.040 | 7 | 76302731 | missense variant | C/T | snv |
|
Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.882 | 0.080 | 7 | 76302962 | missense variant | G/A;C;T | snv | 6.8E-06 |
|
Nervous System Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.080 | 7 | 76303844 | missense variant | G/C;T | snv | 4.0E-06; 4.0E-06 |
|
Nervous System Diseases | 0.700 | 0 |