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

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

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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