ClinVar Miner

Submissions for variant NM_000492.4(CFTR):c.1680-883A>G

dbSNP: rs1554388867
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000672576 SCV000797690 likely pathogenic Cystic fibrosis 2018-02-06 criteria provided, single submitter clinical testing
CFTR-France RCV000672576 SCV001169392 pathogenic Cystic fibrosis 2018-01-29 criteria provided, single submitter curation

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