List of variants in gene DNAH8 reported as likely benign 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_001206927.2(DNAH8):c.11771C>T (p.Thr3924Met)	rs61757218	0.00667
NM_001206927.2(DNAH8):c.13904T>C (p.Met4635Thr)	rs372017066	0.00010
NM_001206927.2(DNAH8):c.10685C>T (p.Thr3562Met)	rs373914023	0.00006
NM_001206927.2(DNAH8):c.8752A>G (p.Ile2918Val)	rs148193715	0.00006
NM_001206927.2(DNAH8):c.3103A>G (p.Ile1035Val)	rs1480696575	0.00001
NM_001206927.2(DNAH8):c.767C>T (p.Ala256Val)	rs776968317	0.00001
NM_001206927.2(DNAH8):c.10971G>A (p.Glu3657=)
NM_001206927.2(DNAH8):c.11888C>T (p.Thr3963Ile)	rs2533609789
NM_001206927.2(DNAH8):c.12249G>A (p.Arg4083=)
NM_001206927.2(DNAH8):c.13573C>A (p.Leu4525Ile)	rs2534080941
NM_001206927.2(DNAH8):c.1648G>A (p.Ala550Thr)	rs748375168
NM_001206927.2(DNAH8):c.2870C>T (p.Thr957Ile)	rs2532424240
NM_001206927.2(DNAH8):c.8834G>A (p.Cys2945Tyr)	rs2533303040

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