List of variants in gene FAT2 reported as uncertain significance for cerebellar ataxia

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001447.3(FAT2):c.1521T>G (p.Ile507Met)	rs1758328376
NM_001447.3(FAT2):c.1653del (p.Leu552fs)
NM_001447.3(FAT2):c.436C>T (p.Pro146Ser)

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