List of variants in gene FGF14 reported as uncertain significance for Autosomal dominant 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_004115.4(FGF14):c.1220_1223dup	rs546246953	0.00062
NM_004115.4(FGF14):c.101_104del	rs886049937
NM_004115.4(FGF14):c.1609_1612del	rs747506157
NM_004115.4(FGF14):c.919_922dup	rs768342824
NM_004115.4(FGF14):c.971_972dup	rs34628929
NM_004115.4(FGF14):c.*972del	rs34628929

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