List of variants in gene DNAH2 reported 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
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_020877.5(DNAH2):c.5265C>G (p.Val1755=)	rs7359662	0.79964
NM_020877.5(DNAH2):c.10799C>T (p.Thr3600Ile)	rs7213894	0.63617
NM_020877.5(DNAH2):c.7950-6C>T	rs1565817	0.53448
NM_020877.5(DNAH2):c.4152C>G (p.Pro1384=)	rs9909288	0.29919
NM_020877.5(DNAH2):c.10169+3G>A	rs872346	0.28090
NM_020877.5(DNAH2):c.5010G>A (p.Ala1670=)	rs62059684	0.23251
NM_020877.5(DNAH2):c.8972+9G>C	rs8073196	0.21412
NM_020877.5(DNAH2):c.294T>C (p.His98=)	rs11867551	0.14235
NM_020877.5(DNAH2):c.4146A>T (p.Ile1382=)	rs9910089	0.03407
NM_020877.5(DNAH2):c.12974C>G (p.Pro4325Arg)	rs116930996	0.02472
NM_020877.5(DNAH2):c.12184A>C (p.Ile4062Leu)	rs79350244	0.02345
NM_020877.5(DNAH2):c.12303A>T (p.Leu4101Phe)	rs117465420	0.02341
NM_020877.5(DNAH2):c.492G>A (p.Arg164=)	rs117035657	0.00887
NM_020877.5(DNAH2):c.2648C>T (p.Ser883Leu)	rs118057786	0.00885
NM_020877.5(DNAH2):c.4453G>C (p.Asp1485His)	rs1060499854

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