"Fulgent Genetics, Fulgent Genetics"[submitter] AND "IL23R"[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 1168829	NM_144701.3(IL23R):c.491+17C>T	IL23R	Single nucleotide variant (intron variant)	Inflammatory bowel disease 17 +2 more	GBenign/Likely benign
Select item 1571673	NM_144701.3(IL23R):c.492-9del	IL23R	Deletion (intron variant)	Inflammatory bowel disease 17 +2 more	GBenign/Likely benign