Variants in gene UMOD with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 14

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HGVS	dbSNP	gnomAD frequency
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.1754C>T (p.Thr585Ile)	rs111992415	0.00382
NM_003361.4(UMOD):c.1062C>T (p.Phe354=)	rs78613713	0.00362
NM_003361.4(UMOD):c.1375C>T (p.Arg459Trp)	rs139607138	0.00146
NM_003361.4(UMOD):c.1406C>T (p.Thr469Met)	rs143583842	0.00051
NM_003361.4(UMOD):c.1464C>T (p.Gly488=)	rs141912637	0.00049
NM_003361.4(UMOD):c.1500A>G (p.Ala500=)	rs200895986	0.00037
NM_003361.4(UMOD):c.1742C>A (p.Thr581Asn)	rs143641292	0.00020
NM_003361.4(UMOD):c.1916T>C (p.Phe639Ser)	rs145165861	0.00016
NM_003361.4(UMOD):c.973+7C>T	rs557659943	0.00014
NM_003361.4(UMOD):c.1623G>T (p.Gly541=)	rs562726925	0.00006
NM_003361.4(UMOD):c.1458C>T (p.Tyr486=)	rs141800038
NM_003361.4(UMOD):c.840C>T (p.Pro280=)	rs78691203

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