ClinVar Miner

Submissions for variant NC_000007.14:g.156789346C>T

gnomAD frequency: 0.42022  dbSNP: rs10949603
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002205651 SCV002364345 benign Holoprosencephaly 3 2025-02-03 criteria provided, single submitter clinical testing

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