"GeneDx"[submitter] AND "LOC130060195"[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Format

Sort by

Choose Destination

Search results

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59583	GRCh38/hg38 17p13.1(chr17:7478195-8435524)x1	ALOX12B, ALOX15B +191 more	Copy number loss	See cases	GPathogenic
Select item 1292220	NM_001139.3(ALOX12B):c.927+110C>T	ALOX12B, LOC130060195	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1282488	NM_001139.3(ALOX12B):c.927+75C>T	ALOX12B, LOC130060195	Single nucleotide variant (intron variant)	not provided	GBenign

Format

Sort by

Choose Destination