List of variants in gene ROR2 reported as likely pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_004560.4(ROR2):c.175+1G>A	rs753069829	0.00001
NM_004560.4(ROR2):c.1970G>A (p.Arg657His)	rs529829552	0.00001
NM_004560.4(ROR2):c.2239C>T (p.Arg747Ter)	rs374646337	0.00001
NM_004560.4(ROR2):c.1083del (p.His362fs)
NM_004560.4(ROR2):c.1868T>C (p.Val623Ala)	rs756550177
NM_004560.4(ROR2):c.1969C>T (p.Arg657Cys)	rs753875871
NM_004560.4(ROR2):c.2264dup (p.Tyr755Ter)	rs1587652899

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