List of variants in gene IFIH1 reported as uncertain significance by Baylor 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_022168.4(IFIH1):c.2016del (p.Asp673fs)	rs773033563	0.00028
NM_022168.4(IFIH1):c.109T>C (p.Phe37Leu)	rs888356659	0.00001
NM_022168.4(IFIH1):c.1015G>A (p.Ala339Thr)	rs1314541924
NM_022168.4(IFIH1):c.2026C>G (p.Leu676Val)	rs1682712829
NM_022168.4(IFIH1):c.2635C>T (p.Gln879Ter)	rs1559809132
NM_022168.4(IFIH1):c.956C>G (p.Ala319Gly)	rs1682931873

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