ClinVar Miner

List of variants reported as uncertain significance for Congenital microvillous atrophy by Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001080467.3(MYO5B):c.1829C>A (p.Ser610Ter)	rs753160864
NM_001080467.3(MYO5B):c.4765G>T (p.Glu1589Ter)	rs762039116
NM_001080467.3(MYO5B):c.613-14_613-11del

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