List of variants in gene IFIH1 reported as benign for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_022168.4(IFIH1):c.2528A>G (p.His843Arg)	rs3747517	0.68382
NM_022168.4(IFIH1):c.2836G>A (p.Ala946Thr)	rs1990760	0.44895
NM_022168.4(IFIH1):c.2616+11T>C	rs3747518	0.16097
NM_022168.4(IFIH1):c.874+109A>G	rs4664463	0.16078
NM_022168.4(IFIH1):c.1525-105C>G	rs2287293	0.13096
NM_022168.4(IFIH1):c.1306+91C>T	rs6734769	0.13094
NM_022168.4(IFIH1):c.1379A>G (p.His460Arg)	rs10930046	0.09666
NM_022168.4(IFIH1):c.2808-75G>T	rs3761652	0.03297
NM_022168.4(IFIH1):c.1524+90G>A	rs16846555	0.03287
NM_022168.4(IFIH1):c.2767A>G (p.Ile923Val)	rs35667974	0.01195
NM_022168.4(IFIH1):c.1641+1G>C	rs35337543	0.00728
NM_022168.4(IFIH1):c.1046A>G (p.Lys349Arg)	rs72650664	0.00111
NM_022168.4(IFIH1):c.2069T>C (p.Leu690Pro)	rs189782013	0.00001
NM_022168.4(IFIH1):c.1095+98_1095+102del	rs141134657
NM_022168.4(IFIH1):c.1306+18dup	rs58630208
NM_022168.4(IFIH1):c.1491G>C (p.Thr497=)	rs12479043
NM_022168.4(IFIH1):c.1765+33T>A	rs4664053

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