"GeneDx"[submitter] AND "LOC129936511"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1189310	NM_017875.4(SLC25A38):c.69+109G>T	LOC129936511, SLC25A38	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1193217	NM_017875.4(SLC25A38):c.69+116A>G	LOC129936511, SLC25A38	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1219552	NM_017875.4(SLC25A38):c.69+182G>A	LOC129936511, SLC25A38	Single nucleotide variant (intron variant)	not provided	GLikely benign

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