Variants in gene FGFR1 with conflicting interpretations "risk factor" and "uncertain significance"

Submission 1 (risk factor) minimum review status:		Submission 1 (risk factor) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 2

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HGVS	dbSNP	gnomAD frequency
NM_023110.3(FGFR1):c.1097C>T (p.Pro366Leu)	rs121909641
NM_023110.3(FGFR1):c.2302G>T (p.Asp768Tyr)	rs121909644

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