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: CA10576326 226382
VCEP: Familial Hypercholesterolemia VCEP
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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
---|---|---|---|---|---|---|---|
View | NM_000527.5(LDLR):c.1955T>C (p.Met652Thr) | Likely Pathogenic | hypercholesterolemia, familial | 2023-10-25 | 1.1 | - | LDLR |
View | NM_000527.5(LDLR):c.1955T>C (p.Met652Thr) | Likely Pathogenic | hypercholesterolemia, familial | 2022-12-23 | 1.0 | - | LDLR |
Showing 1 to 2 of 2 rows