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

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) 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: 9

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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.278_289delinsCCGCCTCCT (p.Val93_Gly97delinsAlaAlaSerCys)	rs878855325
NM_003361.4(UMOD):c.317G>A (p.Cys106Tyr)	rs398123697
NM_003361.4(UMOD):c.376T>C (p.Cys126Arg)	rs121917769
NM_003361.4(UMOD):c.586G>A (p.Asp196Asn)	rs1965729129
NM_003361.4(UMOD):c.610C>G (p.Arg204Gly)	rs1567310019
NM_003361.4(UMOD):c.707C>T (p.Pro236Leu)	rs1447458978
NM_003361.4(UMOD):c.947A>C (p.Gln316Pro)	rs1555487318
NM_003361.4(UMOD):c.949T>G (p.Cys317Gly)	rs1555487316

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