List of variants in gene combination CDCA7L, DNAH11 reported as likely benign for not specified

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001277115.2(DNAH11):c.13495G>A (p.Glu4499Lys)	rs143362381	0.00403
NM_001277115.2(DNAH11):c.13548G>A (p.Ala4516=)	rs147454485	0.00080
NM_001277115.2(DNAH11):c.13305C>T (p.Gly4435=)	rs150682314	0.00029

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