Related gene-specific medical variations for Gene (Select 375061) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2394742	NM_198552.3(FAM89A):c.508C>A (p.Pro170Thr)	FAM89A, MIR1182 (P170T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2276315	NM_198552.3(FAM89A):c.203G>A (p.Gly68Asp)	FAM89A, LOC129932762 (G68D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance