"Institute of Human Genetics, University Hospital Muenster"[submitter] - 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 1708387	NM_001001548.3(CD36):c.120+1G>A	CD36	Single nucleotide variant (splice donor variant +1 more)	Stroke disorder	GPathogenic
Select item 1708388	NM_001001548.3(CD36):c.443T>A (p.Ile148Asn)	CD36 (I114N +2 more)	Single nucleotide variant (missense variant +3 more)	CD36-related condition +1 more	GConflicting classifications of pathogenicity