List of variants in gene DNAH9 reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001372.4(DNAH9):c.6330C>T (p.Asn2110=)	rs3744578	0.73791
NM_001372.4(DNAH9):c.1452A>G (p.Glu484=)	rs9895535	0.42388
NM_001372.4(DNAH9):c.429C>T (p.Pro143=)	rs11078022	0.35841
NM_001372.4(DNAH9):c.9247-14C>T	rs3744586	0.32085
NM_001372.4(DNAH9):c.11982A>G (p.Pro3994=)	rs2286303	0.25123
NM_001372.4(DNAH9):c.12060G>A (p.Thr4020=)	rs1859887	0.25098
NM_001372.4(DNAH9):c.12106G>A (p.Asp4036Asn)	rs17612861	0.24198
NM_001372.4(DNAH9):c.6584A>G (p.Asn2195Ser)	rs3744581	0.20356
NM_001372.4(DNAH9):c.12106-10C>T	rs2286305	0.17418
NM_001372.4(DNAH9):c.13122G>A (p.Met4374Ile)	rs1990236	0.17414
NM_001372.4(DNAH9):c.1810A>G (p.Met604Val)	rs61740059	0.02016
NM_001372.4(DNAH9):c.9543G>A (p.Pro3181=)	rs117483481	0.00323
NM_001372.4(DNAH9):c.3369T>C (p.Asp1123=)	rs8071438
NM_001372.4(DNAH9):c.7513G>T (p.Val2505Leu)	rs61744697
NM_001372.4(DNAH9):c.9744C>G (p.Pro3248=)	rs12449553

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