List of variants reported as uncertain significance for Meckel syndrome by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_153704.6(TMEM67):c.653G>C (p.Gly218Ala)	rs202036490	0.00006
NM_153704.6(TMEM67):c.651+2T>G	rs199821258	0.00003
NM_030578.4(B9D2):c.307C>T (p.Pro103Ser)
NM_030578.4(B9D2):c.496C>G (p.Arg166Gly)
NM_153704.6(TMEM67):c.2557-3T>G	rs1808586167

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