List of variants in gene DNAH5 reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001369.3(DNAH5):c.5658C>T (p.Tyr1886=)	rs6880264	0.01314
NM_001369.3(DNAH5):c.13286G>A (p.Arg4429Gln)	rs61744047	0.00127
NM_001369.3(DNAH5):c.12472C>T (p.Arg4158Trp)	rs3756672	0.00118
NM_001369.3(DNAH5):c.7752+7C>G	rs143848918	0.00116
NM_001369.3(DNAH5):c.894C>G (p.Asn298Lys)	rs116995413	0.00033
NM_001369.3(DNAH5):c.1631C>T (p.Thr544Ile)	rs118026202	0.00031
NM_001369.3(DNAH5):c.360T>C (p.Asp120=)	rs368412855	0.00011
NM_001369.3(DNAH5):c.2307C>T (p.Ala769=)	rs773547505	0.00005
NM_001369.3(DNAH5):c.12171T>C (p.Asp4057=)	rs181510043	0.00004
NM_001369.3(DNAH5):c.10878G>A (p.Thr3626=)	rs188428209	0.00001
NM_001369.3(DNAH5):c.6498A>G (p.Gly2166=)	rs764201218	0.00001
NM_001369.3(DNAH5):c.12033+7A>C	rs77541151
NM_001369.3(DNAH5):c.3873A>T (p.Ile1291=)	rs970611077
NM_001369.3(DNAH5):c.9721-8del	rs560450857

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