C3661900[trait identifier] AND "Functional Genomics, Thrombosis Resear - 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 120088	NM_000698.5(ALOX5):c.996G>A (p.Pro332=)	ALOX5	Single nucleotide variant (synonymous variant)	not provided	Gnot provided
Select item 111275	NM_000895.2(LTA4H):c.*640C>A		Single nucleotide variant	not provided	Gnot provided
Select item 120094	NM_001256643.1(LTA4H):c.88-6908C>T	LTA4H	Single nucleotide variant (intron variant)	not provided	Gnot provided
Select item 120092	NM_001629.4(ALOX5AP):c.323+2451T>C	ALOX5AP	Single nucleotide variant (intron variant)	not provided	Gnot provided

Format

Sort by

Choose Destination