ClinVar Miner

Submissions for variant NM_005655.4(KLF10):c.30G>C (p.Gln10His)

gnomAD frequency: 0.00176  dbSNP: rs145058458
Minimum review status: Collection method:
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 RCV002139671 SCV002419077 likely benign not provided 2025-01-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002139671 SCV005224022 likely benign not provided criteria provided, single submitter not provided

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