ClinVar Miner

List of variants in gene NDUFAF6 reported as pathogenic for inherited Fanconi renotubular syndrome

Included ClinVar conditions (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)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_152416.4(NDUFAF6):c.298-768T>C	rs575462405	0.00004
NM_152416.4(NDUFAF6):c.485del (p.Asn162fs)	rs762093523

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