ClinVar Miner

Submissions for variant NM_017612.5(ZCCHC8):c.200-44T>C

dbSNP: rs7314638
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV002245259 SCV002514090 benign Pulmonary fibrosis and/or bone marrow failure, telomere-related, 5 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004707805 SCV005236440 benign not provided criteria provided, single submitter not provided

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