C0010324[trait identifier] AND "MGZ Medical Genetics Center"[submitter - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1709801	NM_000463.3(UGT1A1):c.1173G>A (p.Met391Ile)	UGT1A7, UGT1A8 +8 more (M123I +4 more)	Single nucleotide variant (missense variant)	Crigler-Najjar syndrome type 1	GUncertain significance
Select item 1709802	NM_000463.3(UGT1A1):c.1208G>T (p.Arg403Leu)	UGT1A3, UGT1A4 +8 more (R135L +4 more)	Single nucleotide variant (missense variant)	Crigler-Najjar syndrome type 1	GUncertain significance