List of variants in gene DNAH5 reported as likely 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001369.3(DNAH5):c.2683G>A (p.Glu895Lys)	rs76229167	0.01663
NM_001369.3(DNAH5):c.3301G>A (p.Val1101Met)	rs61747516	0.01505
NM_001369.3(DNAH5):c.3241A>G (p.Met1081Val)	rs16902880	0.01472
NM_001369.3(DNAH5):c.5658C>T (p.Tyr1886=)	rs6880264	0.01314
NM_001369.3(DNAH5):c.1647C>G (p.Asn549Lys)	rs139160176	0.00831
NM_001369.3(DNAH5):c.6579+6A>G	rs141389162	0.00798
NM_001369.3(DNAH5):c.7752+10T>C	rs149460805	0.00253
NM_001369.3(DNAH5):c.12472C>T (p.Arg4158Trp)	rs3756672	0.00118
NM_001369.3(DNAH5):c.11570+124G>C	rs543104462	0.00057
NM_001369.3(DNAH5):c.4053+13C>T	rs543363871	0.00011
NM_001369.3(DNAH5):c.7465C>T (p.Leu2489=)	rs771511314	0.00002
NM_001369.3(DNAH5):c.1090-8T>C	rs16902950

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