List of variants in gene FIG4 reported as likely benign 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_014845.6(FIG4):c.1242T>C (p.Ile414=)	rs61729087	0.00891
NM_014845.6(FIG4):c.447-16G>T	rs200890189	0.00618
NM_014845.6(FIG4):c.27C>T (p.Ile9=)	rs141040807	0.00398
NM_014845.6(FIG4):c.447-16delinsTT	rs1776038653
NM_014845.6(FIG4):c.447-17dup	rs764540259

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