List of variants in gene SLC25A15 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: 20

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HGVS	dbSNP	gnomAD frequency
NM_014252.4(SLC25A15):c.*515A>G	rs7322603	0.39342
NM_014252.4(SLC25A15):c.*353A>G	rs9549293	0.39328
NM_014252.4(SLC25A15):c.*579C>T	rs7321976	0.39308
NM_014252.4(SLC25A15):c.760A>T (p.Ile254Leu)	rs17849654	0.34875
NM_014252.4(SLC25A15):c.*1855C>A	rs9566580	0.20154
NM_014252.4(SLC25A15):c.333C>T (p.Ala111=)	rs9577152	0.11997
NM_014252.4(SLC25A15):c.*2328G>T	rs9577154	0.08819
NM_014252.4(SLC25A15):c.117G>A (p.Thr39=)	rs41396747	0.08535
NM_014252.4(SLC25A15):c.*929G>C	rs17061602	0.07878
NM_014252.4(SLC25A15):c.*684C>T	rs111782657	0.07643
NM_014252.4(SLC25A15):c.*610G>T	rs7320743	0.07290
NM_014252.4(SLC25A15):c.*1641G>T	rs149457069	0.06406
NM_014252.4(SLC25A15):c.*1626A>G	rs59670947	0.03522
NM_014252.4(SLC25A15):c.*2097T>A	rs17592947	0.03453
NM_014252.4(SLC25A15):c.*48T>A	rs145530626	0.03065
NM_014252.4(SLC25A15):c.*898C>T	rs12585190	0.01899
NM_014252.4(SLC25A15):c.*1945G>A	rs114817943	0.01135
NM_014252.4(SLC25A15):c.*1494A>G	rs113342797	0.01105
NM_014252.4(SLC25A15):c.*420T>G	rs75842883	0.00141
NM_014252.4(SLC25A15):c.*159C>G	rs9577153	0.00139

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