Related gene-specific medical variations for Gene (Select 9862) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2689419	NM_014815.4(MED24):c.291G>C (p.Leu97Phe)	MED24 (L84F +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 599496	NM_014815.4(MED24):c.2288G>A (p.Arg763Gln)	MED24 (R763Q +2 more)	Single nucleotide variant (missense variant +1 more)	Short stature	GLikely pathogenic
Select item 599495	NM_014815.4(MED24):c.1247C>G (p.Thr416Ser)	MED24 (T416S +2 more)	Single nucleotide variant (missense variant +1 more)	Short stature	GLikely pathogenic

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