List of variants in gene DNAH5 reported as benign by Counsyl

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: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001369.3(DNAH5):c.13462C>A (p.Pro4488Thr)	rs113425437	0.03898
NM_001369.3(DNAH5):c.6444+8A>G	rs1348690	0.02931
NM_001369.3(DNAH5):c.1772T>G (p.Leu591Arg)	rs35090077	0.02877
NM_001369.3(DNAH5):c.1395C>T (p.Ser465=)	rs34580014	0.02846
NM_001369.3(DNAH5):c.8449-12T>C	rs111313933	0.02531
NM_001369.3(DNAH5):c.9522G>A (p.Thr3174=)	rs35233147	0.02485
NM_001369.3(DNAH5):c.58-13T>C	rs115758625	0.02407
NM_001369.3(DNAH5):c.12033+7A>G	rs77541151

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.