List of variants in gene DNAH11 reported by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001277115.2(DNAH11):c.8969G>A (p.Arg2990His)	rs72657371	0.01466
NM_001277115.2(DNAH11):c.12561T>G (p.Asp4187Glu)	rs148429731	0.01214
NM_001277115.2(DNAH11):c.3946A>G (p.Met1316Val)	rs17144788	0.01186
NM_001277115.2(DNAH11):c.7812-18C>G	rs147865931	0.00771
NM_001277115.2(DNAH11):c.6416G>A (p.Arg2139Lys)	rs140048925	0.00483
NM_001277115.2(DNAH11):c.13163-19T>A	rs72658832	0.00299
NM_001277115.2(DNAH11):c.11233G>A (p.Glu3745Lys)	rs182389910	0.00242
NM_001277115.2(DNAH11):c.58C>A (p.Arg20Ser)	rs72655967	0.00188
NM_001277115.2(DNAH11):c.8279A>G (p.Gln2760Arg)	rs72657366	0.00108
NM_001277115.2(DNAH11):c.8335C>A (p.Leu2779Met)	rs760409547	0.00004

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