List of variants in gene DNAH11 reported as likely benign by Fulgent Genetics, Fulgent Genetics

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

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_001277115.2(DNAH11):c.5490G>A (p.Leu1830=)	rs55666134	0.11626
NM_001277115.2(DNAH11):c.8188G>T (p.Gly2730Cys)	rs28549882	0.00739
NM_001277115.2(DNAH11):c.693-9T>C	rs72655973	0.00515
NM_001277115.2(DNAH11):c.6041+18T>C	rs72657336	0.00425
NM_001277115.2(DNAH11):c.6067A>G (p.Ile2023Val)	rs72657339	0.00140
NM_001277115.2(DNAH11):c.2542G>A (p.Val848Met)	rs80328282	0.00066
NM_001277115.2(DNAH11):c.6264C>T (p.Pro2088=)	rs187936691	0.00027
NM_001277115.2(DNAH11):c.3843G>A (p.Ala1281=)	rs374551688	0.00008
NM_001277115.2(DNAH11):c.10398C>T (p.Ala3466=)	rs748648201	0.00004
NM_001277115.2(DNAH11):c.7135-18C>T	rs886038472	0.00001
NM_001277115.2(DNAH11):c.13113G>C (p.Pro4371=)	rs148707462
NM_001277115.2(DNAH11):c.4125C>A (p.Arg1375=)	rs570983771

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