ClinVar Miner

Submissions for variant NM_020975.6(RET):c.2136+15G>A

gnomAD frequency: 0.00009  dbSNP: rs751183869
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000411923 SCV000490069 likely benign Multiple endocrine neoplasia type 2B 2016-10-25 criteria provided, single submitter clinical testing
Counsyl RCV000409522 SCV000490070 likely benign Multiple endocrine neoplasia type 2A 2016-10-25 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV000679728 SCV000807023 likely benign not provided 2017-08-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002058862 SCV002406795 benign Multiple endocrine neoplasia, type 2 2024-01-19 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV000411923 SCV004017340 likely benign Multiple endocrine neoplasia type 2B 2023-07-07 criteria provided, single submitter clinical testing

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