"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC129932 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3053876	NM_022786.3(ARV1):c.9C>T (p.Asn3=)	ARV1, LOC129932761	Single nucleotide variant (synonymous variant +1 more)	ARV1-related disorder	GLikely benign
Select item 777986	NM_022786.3(ARV1):c.64A>T (p.Thr22Ser)	ARV1, LOC129932761 (T22S)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GBenign/Likely benign
Select item 734292	NM_022786.3(ARV1):c.73G>T (p.Ala25Ser)	ARV1, LOC129932761 (A25S)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GLikely benign

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ClinVar