List of variants in gene EXOSC9 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_005033.3(EXOSC9):c.522+1G>A	rs151134983	0.00020
NM_005033.3(EXOSC9):c.538C>T (p.Arg180Cys)	rs202225797	0.00007
NM_005033.3(EXOSC9):c.643C>T (p.Arg215Cys)	rs762663826	0.00006
NM_005033.3(EXOSC9):c.206A>G (p.Asn69Ser)	rs761774440	0.00001
NM_005033.3(EXOSC9):c.329dup (p.Arg111fs)	rs754121759	0.00001
NM_005033.3(EXOSC9):c.390G>T (p.Trp130Cys)	rs775495786	0.00001
NM_005033.3(EXOSC9):c.736C>G (p.Gln246Glu)
NM_005033.3(EXOSC9):c.738+5G>C
NM_005033.3(EXOSC9):c.880A>C (p.Thr294Pro)

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