ClinVar Miner

Submissions for variant NM_032273.4(TMEM126A):c.281-13A>C

gnomAD frequency: 0.00001  dbSNP: rs750201466
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002120468 SCV002435815 likely benign not provided 2022-09-30 criteria provided, single submitter clinical testing

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