ClinVar Miner

List of variants reported as risk factor for COVID-19–associated multisystem inflammatory syndrome in children

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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_022168.4(IFIH1):c.1641+1G>C rs35337543 0.00728
NM_006820.4(IFI44L):c.873T>A (p.Tyr291Ter) rs115901054 0.00482
NM_144687.4(NLRP12):c.3046C>T (p.Arg1016Ter) rs35064500 0.00470
NM_003265.3(TLR3):c.889C>G (p.Leu297Val) rs35311343 0.00165
NM_002175.2(IFNA21):c.376G>T (p.Glu126Ter) rs146777169 0.00150
NM_007199.3(IRAK3):c.1461del (p.Asn487fs) rs776951445 0.00071
NM_001289125.3(IFNAR2):c.733G>C (p.Gly245Arg) rs138402252 0.00036
NM_022168.4(IFIH1):c.2016del (p.Asp673fs) rs773033563 0.00028
NM_021068.4(IFNA4):c.60T>A (p.Cys20Ter) rs113055208 0.00022
NM_002348.4(LY9):c.1052_1053del (p.His351fs) rs770956153 0.00017
NM_006417.5(IFI44):c.732C>G (p.Tyr244Ter) rs748188421 0.00009
NM_021002.2(IFNA6):c.187C>T (p.Gln63Ter) rs370196139 0.00003
NM_182985.5(TRIM69):c.1404C>A (p.Phe468Leu) rs201411863 0.00003
NM_001571.6(IRF3):c.1070C>T (p.Pro357Leu) rs200830423 0.00002
NM_006068.5(TLR6):c.337C>T (p.Gln113Ter) rs753476926 0.00001
NM_145725.3(TRAF3):c.1111G>A (p.Ala371Thr) rs551555655 0.00001
NM_001289125.3(IFNAR2):c.1391A>C (p.Asn464Thr) rs1226146327
NM_002176.4(IFNB1):c.403G>T (p.Gly135Ter) rs747015309
NM_003874.4(CD84):c.319del (p.Tyr107fs) rs2102180282
NM_017852.5(NLRP2):c.632dup (p.Tyr212fs) rs2146427557
NM_052962.3(IL22RA2):c.115C>T (p.Arg39Ter) rs201560036
NM_144687.4(NLRP12):c.2828_2829dup (p.Arg944fs) rs533054990
NM_183235.3(RAB27A):c.352C>T (p.Gln118Ter) rs104894500
NM_203416.4(CD163):c.3223C>T (p.Arg1075Ter) rs2136697351

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