List of variants in gene ATP1A2 reported as uncertain significance 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000702.4(ATP1A2):c.1262G>A (p.Arg421Gln)	rs139499540	0.00014
NM_000702.4(ATP1A2):c.1282C>T (p.Arg428Cys)	rs779985796	0.00001
NM_000702.4(ATP1A2):c.1550C>A (p.Thr517Asn)	rs749326394	0.00001
NM_000702.4(ATP1A2):c.1690C>T (p.Arg564Trp)	rs762330744	0.00001
NM_000702.4(ATP1A2):c.192G>T (p.Gln64His)	rs796052282	0.00001
NM_000702.4(ATP1A2):c.2062G>T (p.Ala688Ser)	rs200425518	0.00001
NM_000702.4(ATP1A2):c.2675T>C (p.Met892Thr)	rs794727222	0.00001
NM_000702.4(ATP1A2):c.1097G>A (p.Gly366Asp)	rs1057518514
NM_000702.4(ATP1A2):c.1859C>G (p.Thr620Arg)	rs1057521886
NM_000702.4(ATP1A2):c.2680G>T (p.Asp894Tyr)	rs1553245907
NM_000702.4(ATP1A2):c.2770G>A (p.Val924Met)	rs373276446
NM_000702.4(ATP1A2):c.889G>A (p.Ala297Thr)	rs181618883

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