List of variants reported as uncertain significance for 3M syndrome 3

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_032040.5(CCDC8):c.43C>T (p.Arg15Trp)	rs200189331	0.00022
NM_032040.5(CCDC8):c.287C>G (p.Thr96Arg)	rs758816408	0.00003
NM_032040.5(CCDC8):c.1094A>C (p.Asp365Ala)	rs141966158	0.00001
NM_032040.5(CCDC8):c.1075C>T (p.Gln359Ter)
NM_032040.5(CCDC8):c.43C>G (p.Arg15Gly)	rs200189331
NM_032040.5(CCDC8):c.807del (p.Asn270fs)	rs2513601782
NM_032040.5(CCDC8):c.917_924delinsTCCTATG (p.Glu306fs)	rs2513601440

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