List of variants in gene EXOSC3 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_016042.4(EXOSC3):c.322C>T (p.Arg108Trp)	rs201178873	0.00023
NM_016042.4(EXOSC3):c.674A>G (p.Tyr225Cys)	rs546917405	0.00003
NM_016042.4(EXOSC3):c.476T>C (p.Val159Ala)	rs1247129345	0.00001
NM_016042.4(EXOSC3):c.13G>T (p.Ala5Ser)	rs549030188
NM_016042.4(EXOSC3):c.35T>C (p.Leu12Pro)	rs1447275667
NM_016042.4(EXOSC3):c.420_422del (p.Leu141del)	rs2118980108
NM_016042.4(EXOSC3):c.808_810del (p.Ser270del)	rs755175121
NM_016042.4(EXOSC3):c.94G>A (p.Glu32Lys)	rs941644711

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