List of variants in gene ATP8A2 reported as likely benign for Inborn genetic diseases

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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_016529.6(ATP8A2):c.1757G>A (p.Arg586Gln)	rs202089005	0.00053
NM_016529.6(ATP8A2):c.2292C>T (p.Ile764=)	rs760882012	0.00004
NM_016529.6(ATP8A2):c.2688C>T (p.Phe896=)

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