List of variants in gene RRAS reported as benign for Noonan syndrome

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_006270.5(RRAS):c.344+13G>A	rs1368464	0.71978
NM_006270.5(RRAS):c.333C>T (p.Asn111=)	rs1865077	0.71974
NM_006270.5(RRAS):c.454-10C>G	rs731861	0.23663
NM_006270.5(RRAS):c.397G>A (p.Asp133Asn)	rs61760904	0.00394
NM_006270.5(RRAS):c.408C>T (p.Pro136=)	rs114187560	0.00377
NM_006270.5(RRAS):c.453+20C>T	rs117957448	0.00071
NM_006270.5(RRAS):c.243C>T (p.Ile81=)	rs116683551	0.00063
NM_006270.5(RRAS):c.454-10dup
NM_006270.5(RRAS):c.54A>T (p.Gly18=)	rs571103858

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