ClinVar Miner

Submissions for variant NM_003748.4(ALDH4A1):c.453+19C>T

gnomAD frequency: 0.00609  dbSNP: rs201900829
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002102517 SCV002378958 likely benign Hyperprolinemia type 2 2024-01-17 criteria provided, single submitter clinical testing

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