ClinVar for MedGen (Select 45190) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 635172	NM_000489.6(ATRX):c.4213A>G (p.Arg1405Gly)	ATRX (R1405G +1 more)	Single nucleotide variant (missense variant)	Oligodendroglioma	GUncertain significance
Select item 635171	NM_001386298.1(CIC):c.3017_3018insT (p.Gly1008fs)	CIC (G1008fs +1 more)	Insertion (frameshift variant)	Oligodendroglioma	GLikely pathogenic
Select item 156444	NM_005896.4(IDH1):c.395G>A (p.Arg132His)	IDH1 (R132H)	Single nucleotide variant (missense variant)	Metaphyseal chondromatosis +3 more	GPathogenic/Likely pathogenic

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