ClinVar Miner

Submissions for variant NM_001379500.1(COL18A1):c.3314G>A (p.Arg1105Gln)

gnomAD frequency: 0.00219  dbSNP: rs374207420
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
Invitae RCV001522579 SCV001732154 benign not provided 2024-01-30 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001821841 SCV002065101 likely benign not specified 2020-03-06 criteria provided, single submitter clinical testing

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