List of variants in gene combination FXYD2, FXYD6-FXYD2 reported as uncertain significance by Illumina Laboratory Services, Illumina

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001680.5(FXYD2):c.*124T>A	rs756608243	0.00031
NM_001680.5(FXYD2):c.*149A>G	rs41313497	0.00011
NM_001680.5(FXYD2):c.*188C>T	rs886047704
NM_001680.5(FXYD2):c.36C>G (p.Pro12=)	rs778901593

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