"Illumina Laboratory Services, Illumina"[submitter] AND "IFIH1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1201361	NM_022168.4(IFIH1):c.2558T>C (p.Met853Thr)	IFIH1 (M853T)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 1693291	NM_022168.4(IFIH1):c.2415C>G (p.Ile805Met)	IFIH1 (I805M)	Single nucleotide variant (missense variant)	Aicardi-Goutieres syndrome 7	GUncertain significance
Select item 452793	NM_022168.4(IFIH1):c.77T>A (p.Ile26Asn)	IFIH1 (I26N)	Single nucleotide variant (missense variant)	not specified +3 more	GUncertain significance

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ClinVar