ClinVar Miner

Submissions for variant NM_017565.4(FAM20A):c.1432C>A (p.Arg478=)

gnomAD frequency: 0.00034  dbSNP: rs139620139
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000910918 SCV001055971 likely benign not provided 2023-11-15 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002256594 SCV002535273 benign Hereditary cancer-predisposing syndrome 2021-05-18 criteria provided, single submitter curation

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