ClinVar Miner

Submissions for variant NM_001040167.2(LFNG):c.1002C>T (p.Tyr334=)

gnomAD frequency: 0.03693  dbSNP: rs61743870
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000244913 SCV000306218 benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001523654 SCV001733408 benign Spondylocostal dysostosis 3, autosomal recessive 2024-01-31 criteria provided, single submitter clinical testing
GeneDx RCV001640505 SCV001857946 benign not provided 2018-11-12 criteria provided, single submitter clinical testing

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