"ASTN1-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2639585	NM_004319.3(ASTN1):c.3878A>G (p.Glu1293Gly)	ASTN1 (E1293G +1 more)	Single nucleotide variant (missense variant +1 more)	ASTN1-related condition +1 more	GLikely benign
Select item 3057643	NM_004319.3(ASTN1):c.3734G>A (p.Arg1245His)	ASTN1 (R1245H +1 more)	Single nucleotide variant (missense variant +1 more)	ASTN1-related condition	GLikely benign