ClinVar Miner

Submissions for variant NM_024649.5(BBS1):c.558A>T (p.Val186=)

dbSNP: rs1856039229
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002162446 SCV002332361 likely benign Bardet-Biedl syndrome 2021-03-08 criteria provided, single submitter clinical testing

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