List of variants in gene H3-3B reported as uncertain significance for Inborn genetic diseases

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_005324.5(H3-3B):c.119A>G (p.His40Arg)	rs1555585486
NM_005324.5(H3-3B):c.23C>T (p.Ala8Val)	rs1555585522
NM_005324.5(H3-3B):c.25C>T (p.Arg9Cys)	rs2061653458

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