"GeneDx"[submitter] AND "LOC126862090"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57876	GRCh38/hg38 15q13.3-14(chr15:32326136-39394068)x1	LOC132090301, LOC132090302 +178 more	Copy number loss	See cases	GPathogenic
Select item 57877	GRCh38/hg38 15q13.3-15.1(chr15:32635803-40233825)x1	ACTC1, AQR +219 more	Copy number loss	See cases	GPathogenic
Select item 1233503	NM_001277313.2(FMN1):c.*184C>T	FMN1, LOC126862090	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1238013	NM_001277313.2(FMN1):c.*33G>A	FMN1, LOC126862090	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1267922	NM_001277313.2(FMN1):c.4216-27A>T	FMN1, LOC126862090	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1275341	NM_001277313.2(FMN1):c.4216-171_4216-168del	FMN1, LOC126862090	Microsatellite (intron variant)	not provided	GBenign

ClinVar