ClinVar Miner

Submissions for variant NM_002894.3(RBBP8):c.110-15C>T

gnomAD frequency: 0.00022  dbSNP: rs201687908
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
Invitae RCV002776101 SCV003031623 likely benign not provided 2023-12-26 criteria provided, single submitter clinical testing

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