List of variants reported as likely pathogenic for arthrogryposis syndrome by MGZ Medical Genetics Center

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001999.4(FBN2):c.5917+1del
NM_001999.4(FBN2):c.91C>T (p.Gln31Ter)
NM_018684.4(ZC4H2):c.631C>T (p.Arg211Trp)	rs1555933616

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