List of variants in gene FGF8 reported as likely pathogenic by Muenke lab, National Institutes of Health

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_033163.5(FGF8):c.398C>T (p.Thr133Met)	rs61730334	0.00001
NM_033163.5(FGF8):c.157-1G>A	rs1554834892
NM_033163.5(FGF8):c.157G>C (p.Val53Leu)	rs1554834889
NM_033163.5(FGF8):c.356C>T (p.Thr119Met)	rs876661329
NM_033163.5(FGF8):c.444+1G>A	rs1490604080
NM_033163.5(FGF8):c.469G>T (p.Val157Phe)	rs139565972

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