ClinVar Miner

List of variants in gene IFIH1 reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 40
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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 0.45038
NM_022168.4(IFIH1):c.1095+249C>A rs7565446 0.16100
NM_022168.4(IFIH1):c.1525-313T>C rs7603101 0.16097
NM_022168.4(IFIH1):c.2617-114A>G rs12474565 0.16096
NM_022168.4(IFIH1):c.874+178C>A rs34114189 0.16034
NM_022168.4(IFIH1):c.1095+198T>C rs7591660 0.15431
NM_022168.4(IFIH1):c.874+109A>G rs4664463 0.15327
NM_022168.4(IFIH1):c.874+178_874+179insG rs11455810 0.15286
NM_022168.4(IFIH1):c.1641+244A>C rs2287292 0.15251
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.1524+143C>T rs13431848 0.13069
NM_022168.4(IFIH1):c.1525-149A>G rs7590692 0.12574
NM_022168.4(IFIH1):c.1524+155C>T rs13431841 0.12563
NM_022168.4(IFIH1):c.2455-81_2455-80insT rs113492936 0.11487
NM_022168.4(IFIH1):c.2469C>T (p.Ala823=) rs13418718 0.10215
NM_022168.4(IFIH1):c.2616+198C>A rs13415800 0.10214
NM_022168.4(IFIH1):c.*6G>A rs11891191 0.10208
NM_022168.4(IFIH1):c.1379A>G (p.His460Arg) rs10930046 0.09666
NM_022168.4(IFIH1):c.1765+227T>A rs888284 0.09466
NM_022168.4(IFIH1):c.454-303G>C rs17715343 0.06110
NM_022168.4(IFIH1):c.1766-225G>A rs34977319 0.05702
NM_022168.4(IFIH1):c.1307-62A>T rs58625397 0.05392
NM_022168.4(IFIH1):c.2455-311G>A rs13418892 0.05390
NM_022168.4(IFIH1):c.1307-232C>G rs6731458 0.04054
NM_022168.4(IFIH1):c.2304+91G>C rs76054377 0.03907
NM_022168.4(IFIH1):c.1524+85T>G rs73973094 0.03679
NM_022168.4(IFIH1):c.1524+153T>C rs113687002 0.02396
NM_022168.4(IFIH1):c.2454+6T>C rs6748554 0.02184
NM_022168.4(IFIH1):c.2305-19T>C rs74162085 0.02037
NM_022168.4(IFIH1):c.2455-7T>A rs41399348 0.02035
NM_022168.4(IFIH1):c.1642-206T>C rs112399855 0.01743
NM_022168.4(IFIH1):c.2304+41T>C rs74269124 0.00771
NM_022168.4(IFIH1):c.1306+18dup rs58630208
NM_022168.4(IFIH1):c.1306+25dup rs11441874
NM_022168.4(IFIH1):c.1491G>C (p.Thr497=) rs12479043
NM_022168.4(IFIH1):c.1765+33T>A rs4664053
NM_022168.4(IFIH1):c.454-209TGT[6] rs145943538
NM_022168.4(IFIH1):c.875-180T>G rs6746073

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