List of variants in gene UMOD reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_003361.4(UMOD):c.1740+18C>T	rs113452476	0.00381
NM_003361.4(UMOD):c.1353C>G (p.Gly451=)	rs111904030	0.00378
NM_003361.4(UMOD):c.1062C>T (p.Phe354=)	rs78613713	0.00362
NM_003361.4(UMOD):c.504C>T (p.Leu168=)	rs369454700	0.00014
NM_003361.4(UMOD):c.1383G>A (p.Ala461=)	rs147222401	0.00011
NM_003361.4(UMOD):c.1362C>A (p.Gly454=)	rs770875763	0.00004
NM_003361.4(UMOD):c.114T>C (p.Asn38=)	rs766555124
NM_003361.4(UMOD):c.1577+11G>A	rs184055420
NM_003361.4(UMOD):c.165C>T (p.Gly55=)	rs1478057939
NM_003361.4(UMOD):c.555C>T (p.Arg185=)	rs866510195
NM_003361.4(UMOD):c.840C>T (p.Pro280=)	rs78691203

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