List of variants in gene ROR2 reported as pathogenic by OMIM

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_004560.4(ROR2):c.1324C>T (p.Arg442Ter)	rs267607016	0.00001
NM_004560.4(ROR2):c.1321_1325del (p.Arg441fs)	rs863223290
NM_004560.4(ROR2):c.1366dup (p.Leu456fs)	rs1587657302
NM_004560.4(ROR2):c.1504C>T (p.Gln502Ter)	rs121909083
NM_004560.4(ROR2):c.1937_1943del (p.Tyr646fs)	rs863223291
NM_004560.4(ROR2):c.2160G>A (p.Trp720Ter)	rs121909085
NM_004560.4(ROR2):c.2244del (p.Trp749fs)	rs863223292
NM_004560.4(ROR2):c.2246G>A (p.Trp749Ter)	rs104894122
NM_004560.4(ROR2):c.2247G>A (p.Trp749Ter)	rs104894121
NM_004560.4(ROR2):c.2249del (p.Gly750fs)	rs863223289
NM_004560.4(ROR2):c.2265C>A (p.Tyr755Ter)	rs121909082
NM_004560.4(ROR2):c.355C>T (p.Arg119Ter)	rs121909087
NM_004560.4(ROR2):c.550C>T (p.Arg184Cys)	rs121909084
NM_004560.4(ROR2):c.613C>T (p.Arg205Ter)	rs121909086
NM_004560.4(ROR2):c.622+762_1184-1036del

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