ClinVar Miner

Submissions for variant NM_001174147.2(LMX1B):c.723G>T (p.Ser241=)

dbSNP: rs368736494
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000917538 SCV001062819 likely benign not provided 2022-09-20 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002502783 SCV002809311 likely benign Nail-patella syndrome; Nail-patella-like renal disease 2022-04-14 criteria provided, single submitter clinical testing

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