Related gene-specific medical variations for Gene (Select 55142) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2605772	NM_018097.3(HAUS2):c.89A>G (p.Asn30Ser)	HAUS2, LOC130056925 (N30S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2488670	NM_018097.3(HAUS2):c.34G>A (p.Ala12Thr)	HAUS2, LOC130056925 (A12T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance