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

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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: 15

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HGVS	dbSNP	gnomAD frequency
NM_004115.4(FGF14):c.*1612G>T	rs1046197	0.28765
NM_004115.4(FGF14):c.*471A>C	rs75498912	0.02130
NM_004115.4(FGF14):c.*1063G>A	rs58555898	0.01834
NM_004115.4(FGF14):c.481T>C (p.Leu161=)	rs77082831	0.01311
NM_004115.4(FGF14):c.*31G>A	rs149661933	0.01007
NM_004115.4(FGF14):c.*744C>A	rs79379700	0.00714
NM_004115.4(FGF14):c.*554G>A	rs141793298	0.00557
NM_004115.4(FGF14):c.124G>T (p.Gly42Cys)	rs141304687	0.00191
NM_004115.4(FGF14):c.636T>C (p.His212=)	rs41281644	0.00149
NM_004115.4(FGF14):c.*176C>G	rs191705440	0.00039
NM_004115.4(FGF14):c.*567G>C	rs546536488	0.00007
NM_004115.4(FGF14):c.608-10C>T	rs574476283	0.00001
NM_004115.4(FGF14):c.*1618T>A	rs15608
NM_004115.4(FGF14):c.468C>T (p.Ile156=)	rs558694053
NM_004115.4(FGF14):c.693G>A (p.Ala231=)	rs34397704

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