List of variants in gene DNAH2 reported as uncertain significance for Spermatogenic failure 45

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_020877.5(DNAH2):c.4597C>T (p.Arg1533Cys)
NM_020877.5(DNAH2):c.4701G>T (p.Lys1567Asn)
NM_020877.5(DNAH2):c.8263C>T (p.Arg2755Trp)	rs143616651

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