ClinVar Miner

Submissions for variant NM_015937.6(PIGT):c.594+36dup

dbSNP: rs3092108
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001655291 SCV001867708 benign not provided 2021-03-29 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001788695 SCV002029870 benign Paroxysmal nocturnal hemoglobinuria 2 2021-09-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001788694 SCV002029871 benign Multiple congenital anomalies-hypotonia-seizures syndrome 3 2021-09-05 criteria provided, single submitter clinical testing

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