ClinVar Miner

List of variants in gene EMD reported as uncertain significance for not specified

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Total variants: 10
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HGVS dbSNP
NM_000117.2(EMD):c.229C>T (p.Pro77Ser) rs1557182365
NM_000117.2(EMD):c.272A>G (p.Asn91Ser) rs137977232
NM_000117.2(EMD):c.436G>A (p.Glu146Lys) rs782732591
NM_000117.2(EMD):c.494C>T (p.Thr165Met) rs397515751
NM_000117.2(EMD):c.598T>C (p.Trp200Arg) rs374981936
NM_000117.2(EMD):c.646G>A (p.Gly216Arg) rs147920229
NM_000117.2(EMD):c.70G>A (p.Gly24Arg) rs727504628
NM_000117.2(EMD):c.711C>G (p.Ile237Met) rs727503037
NM_000117.2(EMD):c.73C>A (p.Pro25Thr) rs876661346
NM_000117.2(EMD):c.77T>C (p.Val26Ala) rs727505029

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