List of variants in gene FGF14 reported as benign by Athena Diagnostics Inc

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_004115.4(FGF14):c.481T>C (p.Leu161=)	rs77082831	0.01311
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.373A>G (p.Ile125Val)	rs34073982	0.00135
NM_004115.4(FGF14):c.579A>T (p.Ala193=)	rs138607344	0.00044
NM_004115.4(FGF14):c.123C>T (p.Asn41=)	rs372705140	0.00033
NM_004115.4(FGF14):c.564G>A (p.Lys188=)	rs556509693	0.00004
NM_004115.4(FGF14):c.608-9del	rs558457368
NM_004115.4(FGF14):c.693G>A (p.Ala231=)	rs34397704

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