List of variants in gene SLC25A4 reported as benign for not provided

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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: 17

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HGVS	dbSNP	gnomAD frequency
NM_001151.4(SLC25A4):c.*512A>G	rs7660552	0.90870
NM_001151.4(SLC25A4):c.*2307T>C	rs2046535	0.42438
NM_001151.4(SLC25A4):c.*2943G>A	rs7675110	0.42427
NM_001151.4(SLC25A4):c.*1053T>C	rs55905558	0.42184
NM_001151.4(SLC25A4):c.111+330G>A	rs67596855	0.18294
NM_001151.4(SLC25A4):c.740-293A>G	rs60894332	0.05629
NM_001151.4(SLC25A4):c.112-267T>C	rs58125808	0.05621
NM_001151.4(SLC25A4):c.-25G>A	rs3733652	0.04735
NM_001151.4(SLC25A4):c.*873G>A	rs76680834	0.02960
NM_001151.4(SLC25A4):c.*3114C>A	rs147626367	0.02525
NM_001151.4(SLC25A4):c.681G>A (p.Val227=)	rs34486484	0.00972
NM_001151.4(SLC25A4):c.567T>C (p.Ala189=)	rs149101873	0.00911
NM_001151.4(SLC25A4):c.111+119C>G	rs879317025
NM_001151.4(SLC25A4):c.111+123CGCC[3]	rs143715129
NM_001151.4(SLC25A4):c.111+123CGCC[5]	rs143715129
NM_001151.4(SLC25A4):c.112-65dup	rs34795113
NM_001151.4(SLC25A4):c.112-91dup	rs111595982

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