List of variants in gene DNAH1 reported as uncertain significance by Baylor 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_015512.5(DNAH1):c.9814C>T (p.Arg3272Cys)	rs200784189	0.00085
NM_015512.5(DNAH1):c.11153G>A (p.Arg3718His)	rs371451336	0.00019
NM_015512.5(DNAH1):c.1263G>T (p.Thr421=)	rs111568726	0.00016
NM_015512.5(DNAH1):c.2339G>A (p.Arg780Gln)	rs763577633	0.00002
NM_015512.5(DNAH1):c.3815G>A (p.Arg1272Gln)	rs748124296	0.00002
NM_015512.5(DNAH1):c.6374C>T (p.Thr2125Ile)	rs950353955	0.00002
NM_015512.5(DNAH1):c.10071A>G (p.Leu3357=)	rs554676148	0.00001
NM_015512.5(DNAH1):c.11063A>G (p.Tyr3688Cys)	rs369995851	0.00001
NM_015512.5(DNAH1):c.9854A>G (p.Glu3285Gly)	rs556006237	0.00001
NM_015512.5(DNAH1):c.11338A>G (p.Lys3780Glu)	rs1578207026
NM_015512.5(DNAH1):c.3260G>A (p.Arg1087His)	rs145381093
NM_015512.5(DNAH1):c.6442G>A (p.Gly2148Arg)	rs1314950247

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