ClinVar Miner

Submissions for variant NM_001365536.1(SCN9A):c.1695A>G (p.Gly565=) (rs1574864584)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000866383 SCV001007470 likely benign not provided 2018-03-28 criteria provided, single submitter clinical testing
Invitae RCV001468344 SCV001672386 likely benign Hereditary sensory and autonomic neuropathy type IIA; Generalized epilepsy with febrile seizures plus, type 7 2020-11-30 criteria provided, single submitter clinical testing

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