Related gene-specific medical variations for Gene (Select 126863012) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3178168	NM_014742.4(TM9SF4):c.11C>T (p.Ala4Val)	LOC126863012, TM9SF4 (A4V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2349245	NM_014742.4(TM9SF4):c.7A>G (p.Thr3Ala)	LOC126863012, TM9SF4 (T3A)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GLikely benign