ClinVar Miner

List of variants in gene combination GATM, LOC130056991 reported as uncertain significance for Fanconi renotubular syndrome

Included ClinVar conditions (12):

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001482.3(GATM):c.-1G>A	rs778453861	0.00011
NM_001482.3(GATM):c.61G>A (p.Gly21Arg)	rs903485357	0.00004

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