List of variants in gene FGFR1 reported as not provided for multiple congenital anomalies/dysmorphic syndrome-intellectual disability

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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.91+6G>T	rs886062921	0.00001
NM_023110.3(FGFR1):c.1468G>C (p.Gly490Arg)	rs869025670
NM_023110.3(FGFR1):c.1867G>T (p.Asp623Tyr)	rs398122946
NM_023110.3(FGFR1):c.1880G>C (p.Arg627Thr)	rs869025671
NM_023110.3(FGFR1):c.1884T>G (p.Asn628Lys)	rs869025672
NM_023110.3(FGFR1):c.2174G>A (p.Cys725Tyr)	rs398122945
NM_023110.3(FGFR1):c.494T>C (p.Leu165Ser)	rs397515481
NM_023110.3(FGFR1):c.572T>C (p.Leu191Ser)	rs869025669

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