List of variants in gene ATP2A1 reported as benign for not specified

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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_004320.6(ATP2A1):c.*64G>A	rs10499	0.74014
NM_004320.6(ATP2A1):c.678T>C (p.Thr226=)	rs6565259	0.40633
NM_004320.6(ATP2A1):c.1764+6del	rs66716803	0.06704
NM_004320.6(ATP2A1):c.-22C>T	rs75273069	0.05579
NM_004320.6(ATP2A1):c.2524+3G>T	rs2071341	0.01641
NM_004320.6(ATP2A1):c.1619C>T (p.Pro540Leu)	rs114675305	0.00923
NM_004320.6(ATP2A1):c.1809G>A (p.Pro603=)	rs151309999	0.00800
NM_004320.6(ATP2A1):c.663C>G (p.Gly221=)	rs113803159	0.00468
NM_004320.6(ATP2A1):c.839A>G (p.Asn280Ser)	rs143777158	0.00407
NM_004320.6(ATP2A1):c.1974C>T (p.Phe658=)	rs61626938	0.00306
NM_004320.6(ATP2A1):c.1167C>T (p.Tyr389=)	rs41292388	0.00255
NM_004320.6(ATP2A1):c.870C>T (p.Arg290=)	rs201786788	0.00012
NM_004320.6(ATP2A1):c.1614G>A (p.Thr538=)	rs12596913

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