ClinVar Miner

Submissions for variant NM_006306.4(SMC1A):c.854+17G>A

gnomAD frequency: 0.00004  dbSNP: rs781860125
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002129675 SCV002409984 benign Congenital muscular hypertrophy-cerebral syndrome 2024-01-22 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002500019 SCV002804476 likely benign Congenital muscular hypertrophy-cerebral syndrome; Developmental and epileptic encephalopathy, 85, with or without midline brain defects 2022-02-02 criteria provided, single submitter clinical testing

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