List of variants in gene MAP2K1 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_002755.4(MAP2K1):c.308T>C (p.Ile103Thr)	rs730880502
NM_002755.4(MAP2K1):c.364A>G (p.Asn122Asp)	rs876657651
NM_002755.4(MAP2K1):c.608A>C (p.Glu203Ala)	rs727503996
NM_002755.4(MAP2K1):c.608A>G (p.Glu203Gly)	rs727503996

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