Variants with conflicting interpretations "likely pathogenic" from Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Peking Union Medical College Hospital and "uncertain significance" from any submitter

Minimum review status of the submission from Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Peking Union Medical College Hospital:		Collection method of the submission from Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Peking Union Medical College Hospital:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 4

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HGVS	dbSNP	gnomAD frequency
NM_004560.4(ROR2):c.1675G>A (p.Gly559Ser)	rs117134265	0.00019
NM_002470.4(MYH3):c.4357-10G>A	rs374066994	0.00001
NM_000875.5(IGF1R):c.1732G>A (p.Ala578Thr)	rs2015098252
NM_002470.4(MYH3):c.5658+3_5658+6del	rs2142377032

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