ClinVar Miner

Submissions for variant NM_020975.6(RET):c.337+34C>T

gnomAD frequency: 0.00022  dbSNP: rs368088467
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000411748 SCV000489989 likely benign Multiple endocrine neoplasia, type 2b 2016-09-07 criteria provided, single submitter clinical testing
Counsyl RCV000409765 SCV000489990 likely benign Multiple endocrine neoplasia, type 2a 2016-09-07 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV000411748 SCV004017343 likely benign Multiple endocrine neoplasia, type 2b 2023-07-07 criteria provided, single submitter clinical testing

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