List of variants in gene DNAH9 reported 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
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_001372.4(DNAH9):c.306T>C (p.Phe102=)	rs28507962	0.01633
NM_001372.4(DNAH9):c.8598C>T (p.Ser2866=)	rs61746800	0.00913
NM_001372.4(DNAH9):c.6259A>G (p.Met2087Val)	rs9892290	0.00777
NM_001372.4(DNAH9):c.11284-20A>G	rs113483879	0.00465
NM_001372.4(DNAH9):c.9543G>A (p.Pro3181=)	rs117483481	0.00323
NM_001372.4(DNAH9):c.11921A>T (p.Lys3974Met)	rs111574749	0.00292
NM_001372.4(DNAH9):c.6810C>T (p.His2270=)	rs61732585	0.00267
NM_001372.4(DNAH9):c.6297C>T (p.Pro2099=)	rs143732515	0.00189
NM_001372.4(DNAH9):c.4745+11G>A	rs188575211	0.00050
NM_001372.4(DNAH9):c.39G>C (p.Glu13Asp)	rs186019513	0.00021
NM_001372.4(DNAH9):c.5691G>A (p.Ser1897=)	rs377032791	0.00004
NM_001372.4(DNAH9):c.308del (p.Phe103fs)	rs769795916

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