List of variants reported as benign for Orofacial cleft 6, susceptibility to by Illumina Laboratory Services, Illumina

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 31

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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	0.43246
NM_006147.4(IRF6):c.459G>T (p.Ser153=)	rs2013162	0.36501
NM_006147.4(IRF6):c.*843T>G	rs599021	0.36152
NM_006147.4(IRF6):c.*2151C>A	rs1044516	0.22914
NM_006147.4(IRF6):c.*742A>T	rs742215	0.22621
NM_006147.4(IRF6):c.*1329C>T	rs2235372	0.22609
NM_006147.4(IRF6):c.*840A>G	rs742214	0.22495
NM_006147.4(IRF6):c.*451A>G	rs17317411	0.10461
NM_006147.4(IRF6):c.-75-4A>G	rs2235377	0.04518
NM_006147.4(IRF6):c.820G>A (p.Val274Ile)	rs2235371	0.03768
NM_006147.4(IRF6):c.1153T>C (p.Leu385=)	rs61099902	0.01959
NM_006147.4(IRF6):c.*558C>T	rs73091663	0.01939
NM_006147.4(IRF6):c.*1246C>G	rs58161850	0.01821
NM_006147.4(IRF6):c.*1511C>T	rs114756064	0.01213
NM_006147.4(IRF6):c.*204C>T	rs77906982	0.01138
NM_006147.4(IRF6):c.*353T>C	rs79863693	0.00962
NM_006147.4(IRF6):c.*1265G>C	rs149425923	0.00923
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.*965G>A	rs144692145	0.00261
NM_006147.4(IRF6):c.*2122T>C	rs567043500	0.00258
NM_006147.4(IRF6):c.*2472G>A	rs188593210	0.00199
NM_006147.4(IRF6):c.*279T>C	rs191645857	0.00137
NM_006147.4(IRF6):c.-44G>A	rs2235376	0.00028
NM_006147.4(IRF6):c.*342A>C	rs146078290	0.00009
NM_006147.4(IRF6):c.994G>A (p.Val332Ile)	rs139649287	0.00009
NM_006147.4(IRF6):c.*1771A>G	rs201184204	0.00008
NM_006147.4(IRF6):c.*2597G>A	rs1856161
NM_006147.4(IRF6):c.390G>T (p.Gly130=)	rs34907424

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