ClinVar Miner

Submissions for variant NM_012388.4(BLOC1S6):c.408A>T (p.Ala136=)

dbSNP: rs765691244
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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 RCV002150842 SCV002456561 likely benign Hermansky-Pudlak syndrome 9 2023-10-13 criteria provided, single submitter clinical testing

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