ClinVar Miner

Submissions for variant NM_017654.4(SAMD9):c.2680A>G (p.Lys894Glu)

gnomAD frequency: 0.02332  dbSNP: rs79303965
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000974087 SCV001121898 benign not provided 2025-01-27 criteria provided, single submitter clinical testing
GeneDx RCV000974087 SCV001941220 benign not provided 2019-06-27 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000974087 SCV005268712 benign not provided criteria provided, single submitter not provided
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000974087 SCV005878522 benign not provided 2024-10-17 criteria provided, single submitter clinical testing

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