List of variants in gene combination DNAH11, LOC126859962 reported as likely benign for Primary ciliary dyskinesia

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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001277115.2(DNAH11):c.13069C>A (p.Arg4357=)	rs775720394	0.00006
NM_001277115.2(DNAH11):c.13050-18C>A	rs755689080	0.00001
NM_001277115.2(DNAH11):c.13050-4C>T	rs778868267	0.00001
NM_001277115.2(DNAH11):c.13050-13T>G	rs2534148937
NM_001277115.2(DNAH11):c.13050-14C>G
NM_001277115.2(DNAH11):c.13050-14C>T	rs2534148928
NM_001277115.2(DNAH11):c.13050-18C>T	rs755689080
NM_001277115.2(DNAH11):c.13050-19C>T	rs2128051752
NM_001277115.2(DNAH11):c.13050-8T>C
NM_001277115.2(DNAH11):c.13050-9A>G	rs1209069973
NM_001277115.2(DNAH11):c.13050-9A>T	rs1209069973
NM_001277115.2(DNAH11):c.13053C>T (p.Phe4351=)	rs372123549
NM_001277115.2(DNAH11):c.13055A>G (p.Asn4352Ser)	rs777030468
NM_001277115.2(DNAH11):c.13070G>A (p.Arg4357Gln)	rs369549112

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