List of variants in gene DNAH5 reported as likely benign 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001369.3(DNAH5):c.13338+16C>T	rs115271897	0.01021
NM_001369.3(DNAH5):c.6703T>G (p.Leu2235Val)	rs115109673	0.00961
NM_001369.3(DNAH5):c.6579+20G>A	rs115382993	0.00928
NM_001369.3(DNAH5):c.6919G>A (p.Val2307Ile)	rs74604638	0.00808
NM_001369.3(DNAH5):c.299G>C (p.Gly100Ala)	rs144236383	0.00278
NM_001369.3(DNAH5):c.5272-15dup	rs35337694

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