ClinVar Miner

List of variants reported as likely pathogenic for Pettigrew syndrome

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Total variants: 2

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HGVS	dbSNP
NM_001272071.2(AP1S2):c.321_334del (p.Glu107fs)
NM_003588.3(CUL4B):c.2687G>A (p.Arg896Gln)	rs1556173896

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