List of variants in gene NRAS reported as likely pathogenic 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_002524.5(NRAS):c.108A>G (p.Ile36Met)	rs2101743991
NM_002524.5(NRAS):c.176C>A (p.Ala59Asp)
NM_002524.5(NRAS):c.182A>C (p.Gln61Pro)	rs11554290
NM_002524.5(NRAS):c.204A>T (p.Arg68Ser)
NM_002524.5(NRAS):c.37G>C (p.Gly13Arg)	rs121434595
NM_002524.5(NRAS):c.449A>G (p.Gln150Arg)	rs2101738598

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