List of variants in gene SLC25A4 reported as uncertain significance 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_001151.4(SLC25A4):c.882C>A (p.Ile294=)	rs142164891	0.00005
NM_001151.4(SLC25A4):c.331C>A (p.Arg111Ser)	rs375543860	0.00002
NM_001151.4(SLC25A4):c.755C>T (p.Thr252Met)	rs753197100	0.00002
NM_001151.4(SLC25A4):c.142G>C (p.Glu48Gln)	rs201501984	0.00001
NM_001151.4(SLC25A4):c.228C>T (p.Ala76=)	rs562465418	0.00001
NM_001151.4(SLC25A4):c.371G>A (p.Gly124Glu)	rs863224207	0.00001
NM_001151.4(SLC25A4):c.577G>A (p.Gly193Arg)	rs1553967623	0.00001
NM_001151.4(SLC25A4):c.793G>A (p.Glu265Lys)	rs772055424	0.00001
NM_001151.4(SLC25A4):c.328T>C (p.Trp110Arg)	rs2477169009
NM_001151.4(SLC25A4):c.535G>A (p.Val179Ile)	rs2111285961
NM_001151.4(SLC25A4):c.548G>T (p.Gly183Val)
NM_001151.4(SLC25A4):c.607C>T (p.Pro203Ser)	rs1180189403
NM_001151.4(SLC25A4):c.703C>T (p.Arg235Cys)	rs886041082
NM_001151.4(SLC25A4):c.704G>A (p.Arg235His)	rs1553967679
NM_001151.4(SLC25A4):c.728G>A (p.Gly243Asp)
NM_001151.4(SLC25A4):c.824G>T (p.Trp275Leu)	rs1342164736
NM_001151.4(SLC25A4):c.880A>T (p.Ile294Phe)

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