"Ambry Genetics"[submitter] AND "LOC391322"[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 2259098	NR_186859.1(LOC391322):n.50C>T	LOC391322	Single nucleotide variant	Inborn genetic diseases	GUncertain significance
Select item 2384300	NR_186859.1(LOC391322):n.214T>G	LOC391322	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2399148	NR_186859.1(LOC391322):n.248A>G	LOC391322	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance

Format

Sort by

Choose Destination