List of variants in gene ROR2 reported as pathogenic by GeneDx

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_004560.4(ROR2):c.1324C>T (p.Arg442Ter)	rs267607016	0.00002
NM_004560.4(ROR2):c.1189C>T (p.Arg397Ter)	rs1308509155	0.00001
NM_004560.4(ROR2):c.1366dup (p.Leu456fs)	rs1587657302
NM_004560.4(ROR2):c.2265C>A (p.Tyr755Ter)	rs121909082
NM_004560.4(ROR2):c.566_569dup (p.Ile191fs)	rs1554754007

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