List of variants in gene DNAH5 reported as uncertain significance by Genetics and Molecular Pathology, SA Pathology

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001369.3(DNAH5):c.8757G>C (p.Glu2919Asp)	rs115776799	0.00334
NM_001369.3(DNAH5):c.3514C>A (p.Gln1172Lys)	rs141168110	0.00184
NM_001369.3(DNAH5):c.1121T>C (p.Ile374Thr)	rs147499872	0.00059
NM_001369.3(DNAH5):c.12523G>A (p.Val4175Met)	rs148123430	0.00025
NM_001369.3(DNAH5):c.3315C>A (p.Asn1105Lys)	rs144053917	0.00014
NM_001369.3(DNAH5):c.11456-7C>T
NM_001369.3(DNAH5):c.4199C>T (p.Pro1400Leu)	rs922374480
NM_001369.3(DNAH5):c.6049C>G (p.Arg2017Gly)
NM_001369.3(DNAH5):c.7631C>T (p.Thr2544Met)

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