List of variants in gene FGFR1 reported as likely benign by Ambry 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_023110.3(FGFR1):c.177C>T (p.Asp59=)	rs367880371	0.00035
NM_023110.3(FGFR1):c.1431-5G>A	rs201773631	0.00033
NM_023110.3(FGFR1):c.92-10400G>A	rs367638081	0.00016
NM_023110.3(FGFR1):c.394G>A (p.Asp132Asn)	rs562958780	0.00011
NM_023110.3(FGFR1):c.350A>G (p.Asn117Ser)	rs780765366	0.00005
NM_023110.3(FGFR1):c.937-6T>G	rs374904700	0.00005
NM_023110.3(FGFR1):c.1614C>T (p.Ile538=)	rs747825610	0.00003
NM_023110.3(FGFR1):c.2091C>T (p.Gly697=)	rs773144331	0.00002

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