List of variants in gene ROR2 reported as benign by CeGaT Center for Human Genetics Tuebingen

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_004560.4(ROR2):c.-91G>A	rs141262722	0.00898
NM_004560.4(ROR2):c.717C>T (p.Cys239=)	rs56302651	0.00597
NM_004560.4(ROR2):c.2285C>T (p.Ser762Leu)	rs34491822	0.00357
NM_004560.4(ROR2):c.2805C>G (p.Asp935Glu)	rs41277835

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