List of variants in gene SLC25A3 reported as benign by GeneDx

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_002635.4(SLC25A3):c.814+249G>A	rs2083280	0.99922
NM_002635.4(SLC25A3):c.*211T>A	rs76488843	0.11857
NM_002635.4(SLC25A3):c.460-236C>T	rs74440450	0.05725
NM_002635.4(SLC25A3):c.157+241T>C	rs74933553	0.03140
NM_002635.4(SLC25A3):c.436T>C (p.Leu146=)	rs11544648	0.02958
NM_002635.4(SLC25A3):c.*221T>G	rs115173420	0.02826
NM_002635.4(SLC25A3):c.814+227C>T	rs2372392	0.02596
NM_002635.4(SLC25A3):c.641+171C>G	rs12308813	0.02534
NM_002635.4(SLC25A3):c.459+92T>C	rs12315528	0.01636
NM_002635.4(SLC25A3):c.925+4G>A	rs201617025	0.00194
NM_002635.4(SLC25A3):c.595T>C (p.Leu199=)	rs113045059	0.00112
NM_002635.4(SLC25A3):c.471T>C (p.Tyr157=)	rs531425336	0.00009
NM_002635.4(SLC25A3):c.-38C>G	rs542602103
NM_002635.4(SLC25A3):c.459+31del	rs138634912

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