List of variants in gene DNAH1 studied for not specified

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_015512.5(DNAH1):c.6957C>T (p.His2319=)	rs1546737	0.23926
NM_015512.5(DNAH1):c.3964A>C (p.Arg1322=)	rs11714402	0.18733
NM_015512.5(DNAH1):c.11402G>A (p.Gly3801Asp)	rs12163565	0.15635
NM_015512.5(DNAH1):c.6139-15G>A	rs746239	0.08259
NM_015512.5(DNAH1):c.7151A>G (p.Asn2384Ser)	rs56002041	0.07792
NM_015512.5(DNAH1):c.10881C>A (p.Val3627=)	rs11708581	0.07706
NM_015512.5(DNAH1):c.5332-14G>A	rs375828810	0.00022
NM_015512.5(DNAH1):c.4086G>T (p.Arg1362=)	rs199813499	0.00021
NM_015512.5(DNAH1):c.3432C>T (p.Ser1144=)	rs534534857	0.00013
NM_015512.5(DNAH1):c.3431G>A (p.Ser1144Asn)	rs571987789	0.00003
NM_015512.5(DNAH1):c.7805+6C>T	rs370368596	0.00001
NM_015512.5(DNAH1):c.11495= (p.Arg3832=)	rs1704644099
NM_015512.5(DNAH1):c.4085G>T (p.Arg1362Leu)	rs201355893
NM_015512.5(DNAH1):c.5611-9G>C	rs3752819

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