ClinVar Miner

Submissions for variant NM_000785.4(CYP27B1):c.386+14G>T

dbSNP: rs373607899
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Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002212548 SCV002361849 benign not provided 2024-01-29 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002479878 SCV002799105 benign Vitamin D-dependent rickets, type 1A 2021-07-22 criteria provided, single submitter clinical testing

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