List of variants in gene UMOD reported as uncertain significance for Autosomal dominant medullary cystic kidney disease with or without hyperuricemia

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_003361.4(UMOD):c.1901C>T (p.Thr634Ile)	rs751927256	0.00002
NM_003361.4(UMOD):c.518C>A (p.Pro173Gln)
NM_003361.4(UMOD):c.544G>A (p.Glu182Lys)
NM_003361.4(UMOD):c.698G>T (p.Gly233Val)	rs1965720354
NM_003361.4(UMOD):c.768C>G (p.Cys256Trp)	rs774838407
NM_003361.4(UMOD):c.854C>A (p.Ala285Glu)	rs766919534

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