List of variants in gene DNAH11 reported as benign by Eurofins NTD LLC (GA)

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_001277115.2(DNAH11):c.4377+15A>G	rs57208694	0.50202
NM_001277115.2(DNAH11):c.705C>T (p.Asn235=)	rs10950854	0.45869
NM_001277115.2(DNAH11):c.2454A>G (p.Ala818=)	rs4615458	0.44959
NM_001277115.2(DNAH11):c.101A>T (p.Glu34Val)	rs2285944	0.44667
NM_001277115.2(DNAH11):c.100G>T (p.Glu34Ter)	rs2285943	0.44658
NM_001277115.2(DNAH11):c.7290C>T (p.Phe2430=)	rs12536928	0.42173
NM_001277115.2(DNAH11):c.4449T>C (p.Ile1483=)	rs56029521	0.39493
NM_001277115.2(DNAH11):c.10399G>A (p.Ala3467Thr)	rs2214326	0.38066
NM_001277115.2(DNAH11):c.5621+11A>T	rs59447021	0.23311
NM_001277115.2(DNAH11):c.5490G>A (p.Leu1830=)	rs55666134	0.11626
NM_001277115.2(DNAH11):c.2835A>G (p.Gln945=)	rs17144747	0.07116
NM_001277115.2(DNAH11):c.10739G>A (p.Arg3580His)	rs34879202	0.00942
NM_001277115.2(DNAH11):c.576A>G (p.Ile192Met)	rs72655972	0.00876
NM_001277115.2(DNAH11):c.1426-9T>C	rs72655983	0.00607
NM_001277115.2(DNAH11):c.8266T>C (p.Cys2756Arg)	rs74667361	0.00596
NM_001277115.2(DNAH11):c.640A>G (p.Ile214Val)	rs117064287	0.00595
NM_001277115.2(DNAH11):c.939C>T (p.Ser313=)	rs72655977	0.00522
NM_001277115.2(DNAH11):c.8362C>G (p.His2788Asp)	rs147478795	0.00481
NM_001277115.2(DNAH11):c.9468T>C (p.Asp3156=)	rs201207627	0.00299
NM_001277115.2(DNAH11):c.4430T>C (p.Val1477Ala)	rs72657320	0.00229
NM_001277115.2(DNAH11):c.13076G>A (p.Arg4359Gln)	rs113653972	0.00212
NM_001277115.2(DNAH11):c.10976C>T (p.Ala3659Val)	rs150631721	0.00166
NM_001277115.2(DNAH11):c.11402C>G (p.Pro3801Arg)	rs146362213	0.00061
NM_001277115.2(DNAH11):c.100_101delinsTT (p.Glu34Leu)	rs398123604
NM_001277115.2(DNAH11):c.4378-17_4378-16insATTTA	rs57952953

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