ClinVar Miner

List of variants reported as likely pathogenic for Mental retardation, autosomal dominant 15

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Total variants: 3
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HGVS dbSNP
NM_003073.5(SMARCB1):c.1070C>G (p.Thr357Arg) rs1555881567
NM_003073.5(SMARCB1):c.1087A>G (p.Lys363Glu) rs797045989
NM_003073.5(SMARCB1):c.602G>A (p.Arg201Gln) rs1555877287

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