List of variants in gene FGF14 reported as likely benign for Spinocerebellar ataxia type 27

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_004115.4(FGF14):c.*1259C>T	rs535930764	0.00357
NM_004115.4(FGF14):c.*1118G>A	rs147404825	0.00250
NM_004115.4(FGF14):c.636T>C (p.His212=)	rs41281644	0.00149
NM_004115.4(FGF14):c.123C>T (p.Asn41=)	rs372705140	0.00033
NM_004115.4(FGF14):c.384T>C (p.Asn128=)	rs41281646	0.00029
NM_004115.4(FGF14):c.261C>T (p.Pro87=)	rs757210660	0.00005
NM_004115.4(FGF14):c.*1741T>C	rs529644559	0.00004

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