List of variants in gene combination CEP104, LOC126805586 reported as likely benign by GeneDx

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_014704.4(CEP104):c.1837-258G>A	rs77989248	0.02306
NM_014704.4(CEP104):c.1837-74T>C	rs145970148	0.01257
NM_014704.4(CEP104):c.2043+120G>A	rs79457954	0.00664
NM_014704.4(CEP104):c.1837-251A>G	rs192774445	0.00653
NM_014704.4(CEP104):c.2044-164A>G	rs149317299	0.00555
NM_014704.4(CEP104):c.1966C>T (p.Arg656Cys)	rs148465057	0.00276

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