ClinVar Miner

List of variants in gene WNT5A reported as pathogenic for autosomal dominant Robinow syndrome

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
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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