List of variants in gene UMOD reported as benign by Eurofins NTD LLC (GA)

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_003361.4(UMOD):c.522C>T (p.Cys174=)	rs7193058	0.69325
NM_003361.4(UMOD):c.792G>A (p.Val264=)	rs13335818	0.15554
NM_003361.4(UMOD):c.885G>A (p.Gly295=)	rs28544423	0.15053
NM_003361.4(UMOD):c.-47T>C	rs75645968	0.03162
NM_003361.4(UMOD):c.538C>G (p.Leu180Val)	rs187555378	0.00991
NM_003361.4(UMOD):c.1740+38C>T	rs116674896	0.00897
NM_003361.4(UMOD):c.1372G>T (p.Val458Leu)	rs55772253
NM_003361.4(UMOD):c.1458C>T (p.Tyr486=)	rs141800038
NM_003361.4(UMOD):c.840C>T (p.Pro280=)	rs78691203

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