ClinVar Miner

List of variants in gene combination C1orf122, LOC129930167, YRDC reported as pathogenic for Galloway-Mowat syndrome 10

Included ClinVar conditions (1):

Galloway-Mowat syndrome 10

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)

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_024640.4(YRDC):c.251C>T (p.Ala84Val)	rs1646752498

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