ClinVar Miner

Submissions for variant NM_001201543.2(FAM161A):c.1794A>G (p.Leu598=)

gnomAD frequency: 0.00005  dbSNP: rs78071823
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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 RCV001393190 SCV001594846 likely benign not provided 2024-02-21 criteria provided, single submitter clinical testing

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