Related gene-specific medical variations for Gene (Select 83862) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2588381	NM_031925.3(TMEM120A):c.69C>A (p.Phe23Leu)	LOC129998686, TMEM120A (F23L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2531059	NM_031925.3(TMEM120A):c.17C>T (p.Pro6Leu)	LOC129998686, TMEM120A (P6L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 360732	NM_001395413.1(POR):c.*372G>A	TMEM120A, POR	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +1 more	GUncertain significance

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