ClinVar Miner

List of variants in gene FGF14 reported as likely pathogenic for spinocerebellar ataxia 27A

Included ClinVar conditions (1):

Spinocerebellar ataxia 27A

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: 1

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HGVS	dbSNP	gnomAD frequency
NM_004115.4(FGF14):c.194-1G>C

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