ClinVar for MedGen (Select 934696) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 727441	NM_002447.4(MST1R):c.1861A>T (p.Lys621Ter)	MST1R (K515* +1 more)	Single nucleotide variant (nonsense +1 more)	Nasopharyngeal carcinoma, susceptibility to, 3 +1 more	GBenign/Likely benign
Select item 253185	NM_002447.4(MST1R):c.917G>A (p.Arg306His)	MST1R (R306H)	Single nucleotide variant (missense variant +1 more)	Nasopharyngeal carcinoma, susceptibility to, 3	Grisk factor