List of variants in gene FAH reported as benign for disorder of tyrosine metabolism

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 40

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HGVS	dbSNP	gnomAD frequency
NM_000137.4(FAH):c.553+33A>G	rs1545119	0.73027
NM_000137.4(FAH):c.838-196A>G	rs11072883	0.72099
NM_000137.4(FAH):c.82-74T>C	rs1370276	0.65071
NM_000137.4(FAH):c.961-35C>A	rs2043691	0.61029
NM_000137.4(FAH):c.193-23T>C	rs1370274	0.59414
NM_000137.4(FAH):c.82-13G>A	rs1370275	0.45099
NM_000137.4(FAH):c.455+67T>C	rs2114716	0.43155
NM_000137.4(FAH):c.960+115G>A	rs2162550	0.25281
NM_000137.4(FAH):c.706+79A>G	rs7180031	0.23394
NM_000137.3(FAH):c.*310T>A	rs75212096	0.12315
NM_000137.4(FAH):c.*94T>C	rs1049194	0.12301
NM_000137.4(FAH):c.267G>C (p.Leu89=)	rs33929922	0.07529
NM_000137.3(FAH):c.*284C>G	rs79203348	0.06789
NM_000137.4(FAH):c.1056C>T (p.Ser352=)	rs1801374	0.06041
NM_000137.4(FAH):c.1180+4A>G	rs60585303	0.04595
NM_000137.4(FAH):c.1021C>T (p.Arg341Trp)	rs11555096	0.02131
NM_000137.4(FAH):c.455+29G>A	rs2278204	0.01872
NM_000137.4(FAH):c.*88C>T	rs113381157	0.01818
NM_000137.4(FAH):c.-34C>T	rs142522569	0.01180
NM_000137.4(FAH):c.82-19G>A	rs75733859	0.00966
NM_000137.4(FAH):c.483C>T (p.Gly161=)	rs116272698	0.00943
NM_000137.4(FAH):c.855G>A (p.Pro285=)	rs73481171	0.00927
NM_000137.4(FAH):c.165C>T (p.Leu55=)	rs28733633	0.00811
NM_000137.4(FAH):c.139A>G (p.Lys47Glu)	rs34749737	0.00650
NM_000137.4(FAH):c.554-20T>G	rs199501793	0.00272
NM_000137.4(FAH):c.1098G>A (p.Ser366=)	rs35033541	0.00137
NM_000137.4(FAH):c.921A>G (p.Gly307=)	rs76338717	0.00135
NM_000137.4(FAH):c.961-17G>A	rs372657388	0.00133
NM_000137.4(FAH):c.456-20C>T	rs75021564	0.00128
NM_000137.4(FAH):c.553+10C>T	rs201051426	0.00067
NM_000137.4(FAH):c.181G>T (p.Val61Phe)	rs151264725	0.00053
NM_000137.4(FAH):c.837+9A>T	rs369092208	0.00053
NM_000137.4(FAH):c.81+12G>A	rs200319726	0.00048
NM_000137.4(FAH):c.870C>T (p.Asp290=)	rs377480457	0.00011
NM_000137.4(FAH):c.1209C>T (p.Ile403=)	rs111345782	0.00009
NM_000137.4(FAH):c.314+49G>A	rs1370273
NM_000137.4(FAH):c.455+9T>C	rs531129429
NM_000137.4(FAH):c.543A>G (p.Lys181=)	rs537190415
NM_000137.4(FAH):c.554-15C>T	rs774367598
NM_000137.4(FAH):c.554-16del	rs377104738

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