List of variants in gene ROR2 reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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.75G>A (p.Leu25=)	rs148237260	0.01389
NM_004560.4(ROR2):c.2285C>T (p.Ser762Leu)	rs34491822	0.00357
NM_004560.4(ROR2):c.1959G>A (p.Leu653=)	rs144549032	0.00024
NM_004560.4(ROR2):c.986G>A (p.Ser329Asn)	rs371221714	0.00013
NM_004560.4(ROR2):c.2444C>T (p.Pro815Leu)	rs770921333	0.00005
NM_004560.4(ROR2):c.1687G>A (p.Glu563Lys)	rs186571882	0.00001
NM_004560.4(ROR2):c.1970G>A (p.Arg657His)	rs529829552	0.00001
NM_004560.4(ROR2):c.904C>T (p.Arg302Cys)	rs767372181	0.00001
NM_004560.4(ROR2):c.2805C>G (p.Asp935Glu)	rs41277835
NM_004560.4(ROR2):c.298G>A (p.Ala100Thr)	rs374692105
NM_004560.4(ROR2):c.463+10A>G	rs2118848019

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