List of variants in gene ROR2 reported as likely pathogenic for Brachydactyly type B1; Autosomal recessive Robinow syndrome

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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: 11

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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.1083dup (p.His362fs)
NM_004560.4(ROR2):c.1096C>T (p.Arg366Trp)	rs2118683688
NM_004560.4(ROR2):c.1137del (p.Gln380fs)
NM_004560.4(ROR2):c.1582C>T (p.Arg528Ter)	rs1448877786
NM_004560.4(ROR2):c.1855del (p.Arg619fs)
NM_004560.4(ROR2):c.2018C>G (p.Ser673Ter)
NM_004560.4(ROR2):c.2353del (p.Arg785fs)
NM_004560.4(ROR2):c.550C>T (p.Arg184Cys)	rs121909084
NM_004560.4(ROR2):c.799G>T (p.Glu267Ter)

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