List of variants reported as uncertain significance for Meckel syndrome by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001378615.1(CC2D2A):c.2774G>A (p.Arg925Gln)	rs200707391	0.00061
NM_001378615.1(CC2D2A):c.541G>A (p.Val181Ile)	rs745646755	0.00004
NM_001173990.3(TMEM216):c.431+3A>G
NM_001378615.1(CC2D2A):c.740G>T (p.Gly247Val)
NM_015681.6(B9D1):c.505CTC[1] (p.Leu170del)

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