ClinVar Miner

Submissions for variant NM_020347.4(LZTFL1):c.881+19G>A

gnomAD frequency: 0.00007  dbSNP: rs773028690
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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 RCV001434385 SCV001637190 likely benign not provided 2023-02-24 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002501533 SCV002804864 likely benign Bardet-Biedl syndrome 17 2022-01-12 criteria provided, single submitter clinical testing

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