List of variants in gene WNT5A reported as pathogenic for autosomal dominant 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_003392.7(WNT5A):c.206G>A (p.Cys69Tyr)	rs786204837
NM_003392.7(WNT5A):c.206G>T (p.Cys69Phe)	rs786204837
NM_003392.7(WNT5A):c.248G>C (p.Cys83Ser)	rs786200925
NM_003392.7(WNT5A):c.257A>G (p.Tyr86Cys)	rs786204836
NM_003392.7(WNT5A):c.544T>C (p.Cys182Arg)	rs387906663

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