ClinVar Miner

List of variants reported as uncertain significance for Singleton-Merten syndrome 2

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Total variants: 6
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HGVS dbSNP gnomAD frequency
NM_014314.4(RIGI):c.1232C>T (p.Ser411Leu) rs267602206 0.00001
NM_014314.4(RIGI):c.1863G>T (p.Glu621Asp) rs145874548
NM_014314.4(RIGI):c.2368A>C (p.Ile790Leu) rs771103623
NM_014314.4(RIGI):c.396_399del (p.Asn133fs) rs760088776
NM_014314.4(RIGI):c.816dup (p.Val273fs) rs781124785
NM_014314.4(RIGI):c.877G>C (p.Val293Leu)

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