List of variants in gene WNT5A reported as likely benign 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_003392.7(WNT5A):c.14T>C (p.Ile5Thr)	rs200914260	0.00129
NM_003392.7(WNT5A):c.522G>T (p.Pro174=)	rs559836923	0.00019
NM_003392.7(WNT5A):c.807G>A (p.Lys269=)	rs117338660	0.00016
NM_003392.7(WNT5A):c.502G>A (p.Ala168Thr)	rs572796263	0.00009
NM_003392.7(WNT5A):c.6+18T>A	rs192224802	0.00004
NM_003392.7(WNT5A):c.684+18C>A	rs1264331427	0.00003
NM_003392.7(WNT5A):c.291G>A (p.Ala97=)	rs762941459	0.00001
NM_003392.7(WNT5A):c.*1452AATATA[4]	rs538418882

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