List of variants in gene IFIH1 reported as likely benign by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_022168.4(IFIH1):c.177T>C (p.Val59=)	rs115500208	0.00826
NM_022168.4(IFIH1):c.2807+1G>A	rs35732034	0.00502
NM_022168.4(IFIH1):c.1481G>T (p.Gly494Val)	rs147000317	0.00228
NM_022168.4(IFIH1):c.1046A>G (p.Lys349Arg)	rs72650664	0.00111
NM_022168.4(IFIH1):c.2304+3A>G	rs376806735	0.00027
NM_022168.4(IFIH1):c.2020_2023del (p.Arg674fs)	rs569337014
NM_022168.4(IFIH1):c.875-11A>C	rs186664431

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