List of variants in gene ATP2C2 reported as likely 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_014861.4(ATP2C2):c.304G>A (p.Val102Met)	rs78887288	0.00494
NM_014861.4(ATP2C2):c.1090T>C (p.Leu364=)	rs199936161	0.00039
NM_014861.4(ATP2C2):c.2328G>A (p.Ala776=)	rs186839647	0.00032
NM_014861.4(ATP2C2):c.1123G>A (p.Val375Ile)
NM_014861.4(ATP2C2):c.1644G>A (p.Gly548=)
NM_014861.4(ATP2C2):c.1930-3C>T
NM_014861.4(ATP2C2):c.2227G>T (p.Ala743Ser)	rs373784599
NM_014861.4(ATP2C2):c.378C>A (p.Val126=)

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