List of variants in gene FSCN2 reported by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_012418.4(FSCN2):c.381G>A (p.Pro127=)	rs34454351	0.01717
NM_012418.4(FSCN2):c.49G>A (p.Val17Ile)	rs137853900	0.00240
NM_012418.4(FSCN2):c.1092C>T (p.Ile364=)	rs188142101	0.00195
NM_012418.4(FSCN2):c.1105G>A (p.Gly369Ser)	rs376938035
NM_012418.4(FSCN2):c.829G>A (p.Val277Ile)	rs181420326

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