The ClinGen Evidence Repository is an FDA-recognized human genetic variant database containing expert-curated assertions regarding variants' pathogenicity and supporting evidence summaries.
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Curation History
Variant: CA124487 14948
VCEP: Monogenic Diabetes VCEP
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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_000545.6(HNF1A):c.92G>A (p.Gly31Asp) | Benign | monogenic diabetes | 2022-07-11 | 1.1 | - | HNF1A |
| View | NM_000545.6(HNF1A):c.92G>A (p.Gly31Asp) | Benign | monogenic diabetes | 2021-12-15 | 1.0 | - | HNF1A |
Showing 1 to 2 of 2 rows