ClinVar Miner

List of variants reported as uncertain significance for 3MC syndrome 2 by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_024027.5(COLEC11):c.440G>A (p.Arg147His)	rs746438566	0.00003
NM_024027.5(COLEC11):c.284G>T (p.Gly95Val)	rs2528465394

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