List of variants in gene ATP1A2 reported as benign by Athena Diagnostics Inc

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000702.4(ATP1A2):c.1119G>A (p.Ser373=)	rs1063125	0.18359
NM_000702.4(ATP1A2):c.2961C>T (p.Cys987=)	rs74123254	0.02789
NM_000702.4(ATP1A2):c.1980C>T (p.Cys660=)	rs61734529	0.02220
NM_000702.4(ATP1A2):c.129G>A (p.Lys43=)	rs61734527	0.00766
NM_000702.4(ATP1A2):c.1125G>A (p.Lys375=)	rs61734526	0.00323
NM_000702.4(ATP1A2):c.2967C>T (p.Phe989=)	rs138826759	0.00235
NM_000702.4(ATP1A2):c.340G>A (p.Gly114Ser)	rs116711766	0.00071
NM_000702.4(ATP1A2):c.2751G>A (p.Thr917=)	rs146839867	0.00069
NM_000702.4(ATP1A2):c.339C>T (p.Tyr113=)	rs148929192	0.00023
NM_000702.4(ATP1A2):c.2130C>T (p.Ala710=)	rs374749325	0.00021
NM_000702.4(ATP1A2):c.2273G>C (p.Gly758Ala)	rs147183887	0.00020
NM_000702.4(ATP1A2):c.1652-7C>A	rs200102433
NM_000702.4(ATP1A2):c.1652-7C>G	rs200102433
NM_000702.4(ATP1A2):c.246C>G (p.Pro82=)	rs537472446

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