List of variants in gene FGFR2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000141.5(FGFR2):c.294G>A (p.Thr98=)	rs1047101	0.00776
NM_000141.5(FGFR2):c.159G>A (p.Ala53=)	rs1047102	0.00414
NM_000141.5(FGFR2):c.1788G>A (p.Glu596=)	rs56335660	0.00036
NM_000141.5(FGFR2):c.*674G>T	rs566155088	0.00029
NM_000141.5(FGFR2):c.729G>A (p.Thr243=)	rs199890227	0.00004
NM_000141.5(FGFR2):c.234C>T (p.His78=)	rs778093907	0.00001
NM_000141.5(FGFR2):c.755C>T (p.Ser252Leu)	rs79184941	0.00001
NM_000141.5(FGFR2):c.*197del	rs748777325
NM_000141.5(FGFR2):c.1845G>A (p.Glu615=)
NM_000141.5(FGFR2):c.2302-1589C>T
NM_000141.5(FGFR2):c.2302-1734A>G
NM_000141.5(FGFR2):c.2302-1807_2302-1806insAAAAAAA
NM_000141.5(FGFR2):c.399T>C (p.Asp133=)
NM_000141.5(FGFR2):c.748+182G>A
NM_022970.4(FGFR2):c.1035T>C (p.Tyr345=)

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