List of variants in gene ROR2 reported as benign by Eurofins NTD LLC (GA)

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_004560.4(ROR2):c.*16G>A	rs2230578	0.73170
NM_004560.4(ROR2):c.2455G>A (p.Val819Ile)	rs10761129	0.71630
NM_004560.4(ROR2):c.733A>G (p.Thr245Ala)	rs10820900	0.66416
NM_004560.4(ROR2):c.2088C>T (p.Tyr696=)	rs10992063	0.44353
NM_004560.4(ROR2):c.2154C>T (p.Pro718=)	rs2230577	0.05836
NM_004560.4(ROR2):c.75G>A (p.Leu25=)	rs148237260	0.01389
NM_004560.4(ROR2):c.2727G>A (p.Val909=)	rs56091954	0.01249
NM_004560.4(ROR2):c.937+10C>T	rs201083970	0.00310
NM_004560.4(ROR2):c.1686C>T (p.His562=)	rs56048121	0.00232
NM_004560.4(ROR2):c.2083G>A (p.Gly695Arg)	rs34431454	0.00174
NM_004560.4(ROR2):c.2466C>T (p.Asn822=)	rs146432734	0.00011
NM_004560.4(ROR2):c.1712A>G (p.His571Arg)	rs376970201	0.00005
NM_004560.4(ROR2):c.2805C>G (p.Asp935Glu)	rs41277835

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