Variants in gene UMOD with conflicting interpretations "likely pathogenic" and "uncertain significance"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_003361.4(UMOD):c.317G>T (p.Cys106Phe)	rs398123697	0.00001
NM_003361.4(UMOD):c.326T>A (p.Val109Glu)	rs780462125	0.00001
NM_003361.4(UMOD):c.1382C>A (p.Ala461Glu)	rs780475918
NM_003361.4(UMOD):c.197T>C (p.Leu66Pro)	rs1567311288
NM_003361.4(UMOD):c.533G>C (p.Arg178Pro)	rs1228791562
NM_003361.4(UMOD):c.548A>G (p.Tyr183Cys)	rs1064796542
NM_003361.4(UMOD):c.628G>A (p.Gly210Ser)	rs1567309965

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