ClinVar Miner

Submissions for variant NM_000894.3(LHB):c.233C>A (p.Thr78Asn)

gnomAD frequency: 0.01395  dbSNP: rs116437960
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000947980 SCV001094174 benign not provided 2024-01-15 criteria provided, single submitter clinical testing
GeneDx RCV000947980 SCV001804641 likely benign not provided 2021-02-25 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002502913 SCV002809260 benign Isolated lutropin deficiency 2022-03-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000947980 SCV005209813 likely benign not provided criteria provided, single submitter not provided

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