ClinVar Miner

Submissions for variant NM_004134.7(HSPA9):c.21T>G (p.Ala7=)

gnomAD frequency: 0.00380  dbSNP: rs36043650
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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 RCV000968064 SCV001115494 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002489396 SCV002802896 likely benign Autosomal dominant sideroblastic anemia; Even-plus syndrome 2021-11-23 criteria provided, single submitter clinical testing

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