List of variants reported as uncertain significance for Meckel syndrome by 3billion

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001378615.1(CC2D2A):c.4688C>G (p.Pro1563Arg)	rs886059186	0.00002
NM_017777.4(MKS1):c.959-5C>A	rs765242131
NM_153704.6(TMEM67):c.1174C>T (p.Pro392Ser)

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