ClinVar Miner

Submissions for variant NM_144997.7(FLCN):c.1063-6G>T

dbSNP: rs1060504592
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000470245 SCV000560331 likely benign Birt-Hogg-Dube syndrome 2019-04-24 criteria provided, single submitter clinical testing

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