List of variants in gene IRF6 reported as benign by Illumina Laboratory Services, Illumina

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: 35

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HGVS	dbSNP	gnomAD frequency
NM_006147.4(IRF6):c.*1893C>T	rs680331	0.81024
NM_006147.4(IRF6):c.-73T>C	rs861019	0.43899
NM_006147.4(IRF6):c.*843T>G	rs599021	0.36277
NM_006147.4(IRF6):c.459G>T (p.Ser153=)	rs2013162	0.35925
NM_006147.4(IRF6):c.175-5C>G	rs7552506	0.32118
NM_006147.4(IRF6):c.*742A>T	rs742215	0.22621
NM_006147.4(IRF6):c.*2151C>A	rs1044516	0.22319
NM_006147.4(IRF6):c.*1329C>T	rs2235372	0.22102
NM_006147.4(IRF6):c.*840A>G	rs742214	0.21988
NM_006147.3(IRF6):c.-302A>T	rs12403006	0.15850
NM_006147.4(IRF6):c.*451A>G	rs17317411	0.10461
NM_006147.4(IRF6):c.-75-4A>G	rs2235377	0.03786
NM_006147.4(IRF6):c.820G>A (p.Val274Ile)	rs2235371	0.03768
NM_006147.4(IRF6):c.1153T>C (p.Leu385=)	rs61099902	0.02121
NM_006147.4(IRF6):c.*558C>T	rs73091663	0.01939
NM_006147.4(IRF6):c.*1246C>G	rs58161850	0.01673
NM_006147.4(IRF6):c.*204C>T	rs77906982	0.01225
NM_006147.4(IRF6):c.*1511C>T	rs114756064	0.01213
NM_006147.4(IRF6):c.*1265G>C	rs149425923	0.00992
NM_006147.4(IRF6):c.*353T>C	rs79863693	0.00962
NM_006147.4(IRF6):c.*479T>G	rs75012801	0.00677
NM_006147.4(IRF6):c.*411C>T	rs187379424	0.00492
NM_006147.4(IRF6):c.*665C>A	rs4844899	0.00364
NM_006147.4(IRF6):c.*2122T>C	rs567043500	0.00274
NM_006147.4(IRF6):c.*965G>A	rs144692145	0.00261
NM_006147.4(IRF6):c.*2472G>A	rs188593210	0.00213
NM_006147.4(IRF6):c.*279T>C	rs191645857	0.00138
NM_006147.4(IRF6):c.-44G>A	rs2235376	0.00028
NM_006147.4(IRF6):c.*1771A>G	rs201184204	0.00008
NM_006147.4(IRF6):c.*342A>C	rs146078290	0.00005
NM_006147.4(IRF6):c.994G>A (p.Val332Ile)	rs139649287	0.00001
NM_006147.3(IRF6):c.-313T>A	rs34743335
NM_006147.4(IRF6):c.*1678del	rs141112353
NM_006147.4(IRF6):c.*2597G>A	rs1856161
NM_006147.4(IRF6):c.390G>T (p.Gly130=)	rs34907424

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