ClinVar Miner

Submissions for variant NM_001127644.2(GABRA1):c.74+10C>T

dbSNP: rs557887445
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002539238 SCV001019856 likely benign Idiopathic generalized epilepsy; Epilepsy, idiopathic generalized, susceptibility to, 13; Epilepsy, childhood absence 4 2023-07-14 criteria provided, single submitter clinical testing

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