List of variants in gene ROR2 reported as likely pathogenic for arthrogryposis 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_004560.4(ROR2):c.1675G>A (p.Gly559Ser)	rs117134265	0.00019
NM_004560.4(ROR2):c.808A>G (p.Ile270Val)	rs145631389	0.00017

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