C0017662[trait identifier] AND "NIHR Bioresource Rare Diseases, Univer - 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 813262	Single allele	CFH, KCNT2	Deletion	Mesangiocapillary glomerulonephritis	GLikely pathogenic
Select item 812882	NM_000064.4(C3):c.3085G>A (p.Asp1029Asn)	C3 (D1029N)	Single nucleotide variant (missense variant)	Mesangiocapillary glomerulonephritis	GLikely pathogenic