ClinVar Miner

List of variants in gene GATM reported as benign for primary Fanconi syndrome

Included ClinVar conditions (5):

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.1252T>C (p.Leu418=)	rs1145086	0.55793
NM_001482.3(GATM):c.330A>T (p.Gln110His)	rs1288775	0.45330

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