List of variants reported as uncertain significance for Ellis-van Creveld syndrome by Rare Disease Group, Clinical Genetics,Karolinska Institutet

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Total variants: 4

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HGVS	dbSNP
NM_015650.4(TRAF3IP1):c.1352T>A (p.Leu451His)	rs1559369181
NM_020779.4(WDR35):c.3412G>A (p.Glu1138Lys)	rs978909925
NM_147127.5(EVC2):c.571A>G (p.Asn191Asp)	rs1560228138
NM_181426.2(CCDC39):c.1795C>T (p.Arg599Ter)	rs201780665

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