List of variants in gene DNAH5 reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001369.3(DNAH5):c.5266G>A (p.Glu1756Lys)	rs116524991	0.00282
NM_001369.3(DNAH5):c.4510G>C (p.Gly1504Arg)	rs143567667	0.00277
NM_001369.3(DNAH5):c.10294G>T (p.Val3432Leu)	rs143251588	0.00185
NM_001369.3(DNAH5):c.10323G>A (p.Met3441Ile)	rs149133845	0.00185
NM_001369.3(DNAH5):c.3514C>A (p.Gln1172Lys)	rs141168110	0.00184
NM_001369.3(DNAH5):c.1321-15T>C	rs202081804	0.00160
NM_001369.3(DNAH5):c.8224+15G>A	rs148099176	0.00070
NM_001369.3(DNAH5):c.3534C>T (p.Asn1178=)	rs151274810	0.00046
NM_001369.3(DNAH5):c.11570+8T>C	rs369789559	0.00031
NM_001369.3(DNAH5):c.4687G>A (p.Gly1563Ser)	rs147567352	0.00015
NM_001369.3(DNAH5):c.13492-15T>C	rs192514899	0.00014
NM_001369.3(DNAH5):c.5907T>C (p.Ala1969=)	rs569572855	0.00006
NM_001369.3(DNAH5):c.10545A>G (p.Lys3515=)	rs727502972
NM_001369.3(DNAH5):c.13569C>A (p.Asp4523Glu)	rs151080414
NM_001369.3(DNAH5):c.2578-10_2578-7del	rs71600031
NM_001369.3(DNAH5):c.7212T>C (p.Asp2404=)	rs876657454

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