"PreventionGenetics, part of Exact Sciences"[submitter] AND "ATP6AP2"[ - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 136465	NM_005765.3(ATP6AP2):c.38-5T>C	ATP6AP2	Single nucleotide variant (intron variant)	ATP6AP2-related condition +4 more	GBenign/Likely benign
Select item 697712	NM_005765.3(ATP6AP2):c.472C>T (p.Leu158=)	ATP6AP2	Single nucleotide variant (synonymous variant)	ATP6AP2-related condition +2 more	GLikely benign
Select item 2810452	NM_005765.3(ATP6AP2):c.858+4A>G	ATP6AP2	Single nucleotide variant (intron variant)	ATP6AP2-related condition +1 more	GUncertain significance

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