List of variants in gene FGFR1 reported as benign by Clinical Genetics, Academic Medical Center

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_023110.3(FGFR1):c.2187-6C>T	rs4647904	0.01503
NM_023110.3(FGFR1):c.2314C>T (p.Pro772Ser)	rs56234888	0.01307
NM_023110.3(FGFR1):c.600C>T (p.Asp200=)	rs17175898	0.00761
NM_023110.3(FGFR1):c.345C>T (p.Ser115=)	rs2915665	0.00567
NM_023110.3(FGFR1):c.449-9C>G	rs17182303	0.00109
NM_023110.3(FGFR1):c.320C>T (p.Ser107Leu)	rs140382957	0.00062
NM_023110.3(FGFR1):c.75G>A (p.Pro25=)	rs17175757	0.00010

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