List of variants in gene TF reported as benign for inherited deficiency anemia

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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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001063.4(TF):c.-2A>G	rs1130459	0.57926
NM_001063.4(TF):c.1572G>C (p.Leu524=)	rs8649	0.26591
NM_001063.4(TF):c.624G>A (p.Ser208=)	rs12769	0.26134
NM_001063.4(TF):c.1765C>T (p.Pro589Ser)	rs1049296	0.13332
NM_001063.4(TF):c.739C>T (p.Leu247=)	rs1799852	0.10437
NM_001063.3(TF):c.-84G>T	rs8177186	0.07960
NM_001063.4(TF):c.804T>C (p.His268=)	rs8177232	0.05865
NM_001063.4(TF):c.829G>A (p.Gly277Ser)	rs1799899	0.04529
NM_001063.4(TF):c.887A>G (p.Asp296Gly)	rs8177238	0.01230
NM_001063.4(TF):c.1614C>T (p.Gly538=)	rs8177286	0.01173
NM_001063.4(TF):c.582A>G (p.Pro194=)	rs8177226	0.01102
NM_001063.4(TF):c.432C>T (p.Ser144=)	rs41298987	0.01050
NM_001063.4(TF):c.417G>A (p.Thr139=)	rs113868497	0.00362
NM_001063.4(TF):c.216+14G>C	rs114449208	0.00299
NM_001063.4(TF):c.635+13T>A	rs41298993	0.00246
NM_001063.4(TF):c.956A>G (p.His319Arg)	rs41295774	0.00224

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