ClinVar Miner

List of variants reported as uncertain significance for Orofacial cleft 6, susceptibility to

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Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_006147.4(IRF6):c.*575T>A rs561885624 0.00066
NM_006147.4(IRF6):c.*932A>G rs776408684 0.00063
NM_006147.4(IRF6):c.*591T>G rs576516344 0.00021
NM_006147.4(IRF6):c.*2795G>A rs760763242 0.00012
NM_006147.4(IRF6):c.*515G>A rs182317104 0.00009
NM_006147.4(IRF6):c.*1473C>G rs531092939 0.00008
NM_006147.4(IRF6):c.*2268C>T rs752399888 0.00006
NM_006147.4(IRF6):c.*2344C>T rs866747914 0.00006
NM_006147.4(IRF6):c.*1767G>A rs886045878 0.00005
NM_006147.4(IRF6):c.*2006T>C rs1468618309 0.00005
NM_006147.4(IRF6):c.*2002A>G rs1050174407 0.00004
NM_006147.4(IRF6):c.*2658A>C rs1428189240 0.00004
NM_006147.4(IRF6):c.1007T>G (p.Leu336Arg) rs761816133 0.00004
NM_006147.4(IRF6):c.*1172T>A rs926144526 0.00003
NM_006147.4(IRF6):c.*2064G>A rs886045876 0.00003
NM_006147.4(IRF6):c.-98T>C rs886045886 0.00002
NM_006147.4(IRF6):c.1321C>T (p.Arg441Cys) rs1234188725 0.00002
NM_006147.4(IRF6):c.888C>T (p.Asp296=) rs748882482 0.00002
NM_006147.4(IRF6):c.*1276C>T rs930043539 0.00001
NM_006147.4(IRF6):c.-75-15C>T rs191103054 0.00001
NM_006147.4(IRF6):c.313A>G (p.Met105Val) rs1032249718 0.00001
NM_006147.4(IRF6):c.508+13G>A rs781129893 0.00001
NM_006147.4(IRF6):c.*1123T>C rs886045879
NM_006147.4(IRF6):c.*1474C>T rs895818762
NM_006147.4(IRF6):c.*1585C>T rs1047020008
NM_006147.4(IRF6):c.*1700G>A rs575407072
NM_006147.4(IRF6):c.*1700G>C rs575407072
NM_006147.4(IRF6):c.*1712T>C rs1050315474
NM_006147.4(IRF6):c.*1844G>A rs886045877
NM_006147.4(IRF6):c.*1870G>C rs2077834990
NM_006147.4(IRF6):c.*1999T>C rs2077834086
NM_006147.4(IRF6):c.*477G>A rs763919560
NM_006147.4(IRF6):c.*804C>G rs917524521
NM_006147.4(IRF6):c.-3-11G>C rs886045885
NM_006147.4(IRF6):c.1065C>T (p.Leu355=) rs1317826948
NM_006147.4(IRF6):c.1107T>A (p.Phe369Leu) rs2102536039
NM_006147.4(IRF6):c.1388C>T (p.Ala463Val) rs886045883
NM_006147.4(IRF6):c.598A>G (p.Met200Val) rs886045884

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