ClinVar Miner

Submissions for variant NM_001201543.2(FAM161A):c.1488G>A (p.Lys496=)

dbSNP: rs1572877944
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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 RCV000945196 SCV001091186 likely benign not provided 2018-08-27 criteria provided, single submitter clinical testing

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