List of variants in gene USB1 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_024598.4(USB1):c.641G>A (p.Cys214Tyr)	rs146685901	0.00223
NM_024598.4(USB1):c.784A>G (p.Met262Val)	rs143382202	0.00027
NM_024598.4(USB1):c.734G>A (p.Arg245His)	rs140289507	0.00021
NM_024598.4(USB1):c.213G>A (p.Val71=)	rs369515724	0.00006
NM_024598.4(USB1):c.646G>A (p.Gly216Ser)	rs778666156	0.00005
NM_024598.4(USB1):c.100G>A (p.Gly34Ser)	rs769630452	0.00003
NM_024598.4(USB1):c.253G>A (p.Val85Ile)	rs764580227	0.00002
NM_024598.4(USB1):c.208C>T (p.Arg70Trp)	rs531886363
NM_024598.4(USB1):c.277G>A (p.Glu93Lys)	rs2142302137
NM_024598.4(USB1):c.61G>A (p.Gly21Arg)	rs778756392

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