List of variants in gene ATP13A2 reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_022089.4(ATP13A2):c.145G>A (p.Gly49Ser)	rs56379718	0.00681
NM_022089.4(ATP13A2):c.132A>G (p.Pro44=)	rs200816691	0.00471
NM_022089.4(ATP13A2):c.3235+20C>T	rs376475762	0.00044
NM_022089.4(ATP13A2):c.3087C>T (p.Phe1029=)	rs184878897	0.00039
NM_022089.4(ATP13A2):c.844A>T (p.Ser282Cys)	rs538497077	0.00010
NM_022089.4(ATP13A2):c.2529+9G>A	rs200809857	0.00006
NM_022089.4(ATP13A2):c.2151C>T (p.Ser717=)	rs544545629

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