Related gene-specific medical variations for Gene (Select 89927) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3134486	NM_033201.3(BMERB1):c.560C>T (p.Thr187Met)	BMERB1, MPV17L-BMERB1 (T170M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134485	NM_033201.3(BMERB1):c.232A>G (p.Met78Val)	BMERB1, MPV17L-BMERB1 (M61V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance