List of variants in gene ATP2B4 reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001684.5(ATP2B4):c.3158C>T (p.Ser1053Phe)	rs148156799	0.00862
NM_001684.5(ATP2B4):c.1122G>A (p.Thr374=)	rs2229564	0.00240
NM_001684.5(ATP2B4):c.1981G>A (p.Glu661Lys)	rs147729934	0.00150
NM_001684.5(ATP2B4):c.3152C>A (p.Thr1051Asn)	rs61825652	0.00105
NM_001684.5(ATP2B4):c.1674C>T (p.Pro558=)

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