ClinVar for MedGen (Select 9030) - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Format

Sort by

Choose Destination

Links from MedGen

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1195988	NM_002880.4(RAF1):c.673C>T (p.Pro225Ser)	RAF1 (P144S +1 more)	Single nucleotide variant (intron variant +2 more)	Glioma	GBenign
Select item 1195985	t(12;15)(p13;q25)	NTRK3	Variation	Glioma	GPathogenic
Select item 930214	t(10;16)(q26;q11)	FGFR2, VPS35	Translocation	Glioma	GLikely pathogenic
Select item 617751	Single allele	ABHD17B, ACO1 +185 more	Complex	Glioma	GLikely pathogenic

Format

Sort by

Choose Destination