List of variants in gene FGFR2 reported as benign for not specified

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_000141.5(FGFR2):c.2301+15C>T	rs2278202	0.45747
NM_000141.5(FGFR2):c.*259C>T	rs1047057	0.43446
NM_000141.5(FGFR2):c.1864-125dup	rs4647914	0.28147
NM_000141.5(FGFR2):c.1864-43del	rs111564057	0.17733
NM_000141.5(FGFR2):c.-157A>G	rs41258305	0.13622
NM_000141.5(FGFR2):c.557T>C (p.Met186Thr)	rs755793	0.10553
NM_000141.5(FGFR2):c.1941C>T (p.Leu647=)	rs35337478	0.02240
NM_000141.5(FGFR2):c.1864-17T>G	rs3135802	0.02120
NM_000141.5(FGFR2):c.110-54C>T	rs3135732	0.01267
NM_000141.5(FGFR2):c.109+10T>G	rs3135722	0.00799
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.1572A>G (p.Thr524=)	rs74160613	0.00298
NM_000141.5(FGFR2):c.170C>T (p.Ser57Leu)	rs56226109	0.00271
NM_000141.5(FGFR2):c.17G>C (p.Arg6Pro)	rs3750819	0.00250
NM_000141.5(FGFR2):c.23T>G (p.Ile8Ser)	rs147307031	0.00107
NM_000141.5(FGFR2):c.1986+7C>T	rs199697707	0.00032
NM_000141.5(FGFR2):c.1084+8C>T	rs1589827584
NM_000141.5(FGFR2):c.696A>G (p.Val232=)	rs1047100

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