Related gene-specific medical variations for Gene (Select 88455) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3122927	NM_033121.2(ANKRD13A):c.1066A>G (p.Arg356Gly)	ANKRD13A, LOC126861636 (R356G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287220	NM_033121.2(ANKRD13A):c.967A>G (p.Thr323Ala)	ANKRD13A, LOC126861636 (T323A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267639	NM_033121.2(ANKRD13A):c.28C>A (p.His10Asn)	ANKRD13A, GIT2 (H10N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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