List of variants reported as uncertain significance for multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome by Institute of Human Genetics, University Hospital of Duesseldorf

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_017780.4(CHD7):c.500C>T (p.Pro167Leu)	rs61742851	0.00002
NM_003392.7(WNT5A):c.157A>T (p.Asn53Tyr)
NM_017780.4(CHD7):c.2836-15C>G
NM_019066.5(MAGEL2):c.2941C>T (p.Leu981Phe)

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