C1853120[trait identifier] AND "Institute of Human Genetics, Universit - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1285405	NM_005633.4(SOS1):c.1289A>G (p.Asp430Gly)	SOS1 (D423G +1 more)	Single nucleotide variant (missense variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 376542	NM_005633.4(SOS1):c.697A>T (p.Asn233Tyr)	SOS1 (N233Y +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 4	GLikely pathogenic
Select item 975988	NM_005633.4(SOS1):c.427A>G (p.Lys143Glu)	SOS1 (K136E +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 4	GUncertain significance

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