Related gene-specific medical variations for Gene (Select 57862) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2244563	NM_021188.3(ZNF410):c.1295G>T (p.Arg432Leu)	FAM161B, ZNF410 (R359L +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2213531	NM_021188.3(ZNF410):c.1295G>A (p.Arg432His)	FAM161B, ZNF410 (R236H +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance