List of variants in gene ROR2 reported as benign by PreventionGenetics, part of Exact Sciences

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: 11

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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.494+25G>A	rs12683181	0.68697
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.98-15G>C	rs7863557	0.22863
NM_004560.4(ROR2):c.938-33C>T	rs10992070	0.09787
NM_004560.4(ROR2):c.498T>C (p.Asp166=)	rs16907720	0.09084
NM_004560.4(ROR2):c.2154C>T (p.Pro718=)	rs2230577	0.05836
NM_004560.4(ROR2):c.1710G>A (p.Pro570=)	rs41277837	0.02804
NM_004560.4(ROR2):c.1686C>T (p.His562=)	rs56048121	0.00232

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