Source: NCBI ClinVar ( ID 1032122 )
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Variation set ID | Names | Clinical significance | Review status | Last evaluated | Releated variation |
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Interpretation ID | Variation set ID | Clinical significance | Condition | Phenotype | Review status | Last evaluated | Submitter | Comment |
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Origin | Ethnicity | Affetcted | Literature | Method | Description | Interpretation id |
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Call ID | Assembly | Chr | Start | End | Validation | Copy number | Zygosity | Origin | Phenotype | HGVS/Genome Variation | Coverage | Description |
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Call ID | Population name | Population class | Group | Allele: frequency (count) | Genotype: frequency (count) |
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Project ID | Title | Data type | Accession in other database | Release date | Description |
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Sample ID | Sample name | Sample title | Organism | Sample type | Related accession | Accession in other database | Release date | Description |
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Experiment ID | Title | Platform | Strategy | Source | Selection | Related accession | Accession in other database | Release date |
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