List of variants in gene FGFR1 reported as benign for not provided

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: 35

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_023110.3(FGFR1):c.-88-3285C>G	rs13275043	0.44467
NM_023110.3(FGFR1):c.1855-123G>C	rs4647905	0.20097
NM_023110.3(FGFR1):c.1855-163G>T	rs4647903	0.19396
NM_023110.3(FGFR1):c.92-89G>A	rs4647907	0.19288
NM_023110.3(FGFR1):c.622-248G>A	rs2293971	0.18320
NM_023110.3(FGFR1):c.359-272C>T	rs2288696	0.16739
NM_023110.3(FGFR1):c.746-77G>A	rs2280846	0.07488
NM_023110.3(FGFR1):c.-385G>A	rs2467531	0.06909
NM_023110.3(FGFR1):c.746-272A>C	rs17175940	0.02092
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	0.00782
NM_023110.3(FGFR1):c.2262G>A (p.Leu754=)	rs56341011	0.00711
NM_023110.3(FGFR1):c.345C>T (p.Ser115=)	rs2915665	0.00567
NM_023110.3(FGFR1):c.-88-1068C>G	rs17182148	0.00437
NM_023110.3(FGFR1):c.449-25G>C	rs141320658	0.00306
NM_023110.3(FGFR1):c.2292+36G>A	rs17176067	0.00192
NM_023110.3(FGFR1):c.336C>T (p.Thr112=)	rs148480919	0.00153
NM_023110.3(FGFR1):c.449-9C>G	rs17182303	0.00115
NM_023110.3(FGFR1):c.1081+20C>T	rs17175982	0.00092
NM_023110.3(FGFR1):c.1098G>A (p.Pro366=)	rs56174879	0.00079
NM_023110.3(FGFR1):c.-89+499G>A	rs545215318	0.00056
NM_023110.3(FGFR1):c.168G>A (p.Arg56=)	rs147482922	0.00021
NM_023110.3(FGFR1):c.*66G>A	rs866523242
NM_023110.3(FGFR1):c.-89+278T>C
NM_023110.3(FGFR1):c.-89+3064G>T
NM_023110.3(FGFR1):c.-89+3248T>A
NM_023110.3(FGFR1):c.2293-6T>C	rs2150512800
NM_023110.3(FGFR1):c.359-89G>A	rs2150935912
NM_023110.3(FGFR1):c.618C>T (p.Tyr206=)	rs2150909450
NM_023110.3(FGFR1):c.622-25G>C	rs2150868012
NM_023110.3(FGFR1):c.873G>A (p.Lys291=)	rs2150817700
NM_023110.3(FGFR1):c.92-287_92-286insTGATC	rs10678546
NM_023110.3(FGFR1):c.936+46A>T	rs2150809832
NM_023110.3(FGFR1):c.937-77T>C	rs2150763363

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.