ClinVar Miner

List of variants reported as uncertain significance for TARP syndrome

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_005676.5(RBM10):c.1476G>T (p.Ser492=)	rs138358884
NM_005676.5(RBM10):c.856G>A (p.Ala286Thr)
NM_005676.5(RBM10):c.995G>A (p.Arg332His)

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