ClinVar Miner

Submissions for variant NM_020975.6(RET):c.1879+17C>T

gnomAD frequency: 0.00010  dbSNP: rs369920430
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000409720 SCV000489907 likely benign Multiple endocrine neoplasia type 2B 2016-07-28 criteria provided, single submitter clinical testing
Counsyl RCV000410729 SCV000489908 likely benign Multiple endocrine neoplasia type 2A 2016-07-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002058858 SCV002407136 benign Multiple endocrine neoplasia, type 2 2024-01-31 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV000409720 SCV004017351 likely benign Multiple endocrine neoplasia type 2B 2023-07-07 criteria provided, single submitter clinical testing

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