List of variants reported as pathogenic for Seckel syndrome 5 by OMIM

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001194998.2(CEP152):c.2000A>G (p.Lys667Arg)	rs200879436	0.00450
NM_001194998.2(CEP152):c.2034T>G (p.Tyr678Ter)	rs182018947	0.00048
NM_001194998.2(CEP152):c.261+1G>C	rs966888627
NM_001194998.2(CEP152):c.2694+1G>T	rs1349385657
NM_001194998.2(CEP152):c.4378_4379del (p.Val1460fs)	rs141600901

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