List of variants in gene WNT5A reported as likely 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_003392.7(WNT5A):c.247T>G (p.Cys83Gly)	rs2106946273
NM_003392.7(WNT5A):c.248G>A (p.Cys83Tyr)	rs786200925
NM_003392.7(WNT5A):c.461G>T (p.Cys154Phe)	rs2051315439
NM_003392.7(WNT5A):c.479C>G (p.Ser160Cys)	rs1553677971
NM_003392.7(WNT5A):c.487G>C (p.Gly163Arg)	rs587784562
NM_003392.7(WNT5A):c.487_492dup (p.Gly163_Cys164dup)	rs1553677967

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