ClinVar Miner

Submissions for variant NC_000007.14:g.156769398G>C

gnomAD frequency: 0.00150  dbSNP: rs76709606
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 RCV002183776 SCV002478954 benign Holoprosencephaly 3 2024-12-20 criteria provided, single submitter clinical testing

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