ClinVar Miner

List of variants in gene FIG4 reported as likely pathogenic by Mayo Clinic Laboratories, Mayo Clinic

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_014845.6(FIG4):c.2547-1G>A	rs769858739	0.00001
NM_014845.6(FIG4):c.592C>T (p.Gln198Ter)	rs745554323	0.00001

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