ClinVar Miner

Submissions for variant NM_001174147.2(LMX1B):c.327-6C>T

dbSNP: rs572751023
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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 RCV002209827 SCV002361823 likely benign not provided 2021-10-14 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002498221 SCV002808495 likely benign Nail-patella syndrome; Nail-patella-like renal disease 2022-03-03 criteria provided, single submitter clinical testing

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