ClinVar Miner

Submissions for variant NM_004448.4(ERBB2):c.3573G>A (p.Val1191=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003086860 SCV003485426 likely benign not provided 2023-03-19 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005021573 SCV005646018 uncertain significance Glioma susceptibility 1; Ovarian cancer; Gastric cancer; Lung cancer; Visceral neuropathy, familial, 2, autosomal recessive 2024-01-19 criteria provided, single submitter clinical testing

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