"Fulgent Genetics, Fulgent Genetics"[submitter] AND "LOC130061383"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 890948	NM_000789.4(ACE):c.231G>A (p.Ala77=)	ACE, LOC130061383	Single nucleotide variant (synonymous variant)	Renal tubular dysgenesis +4 more	GBenign/Likely benign
Select item 1630344	NM_000789.4(ACE):c.249+15C>G	ACE, LOC130061383	Single nucleotide variant (intron variant)	not provided +3 more	GLikely benign
Select item 1630345	NM_000789.4(ACE):c.249+16C>G	ACE, LOC130061383	Single nucleotide variant (intron variant)	Microvascular complications of diabetes, susceptibility to, 3 +3 more	GLikely benign

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ClinVar