List of variants in gene PRICKLE2 reported as uncertain significance for electroclinical syndrome

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_198859.4(PRICKLE2):c.1706G>A (p.Arg569Gln)	rs2076627525	0.00001
NM_198859.4(PRICKLE2):c.2246C>T (p.Pro749Leu)	rs762399074	0.00001

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