ClinVar Miner

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

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Gene type:
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Total variants: 76
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HGVS dbSNP gnomAD frequency
NM_000141.5(FGFR2):c.2301+1716A>G rs1649167 0.98736
NM_000141.5(FGFR2):c.749-183G>A rs2981447 0.89019
NM_000141.5(FGFR2):c.749-62G>A rs2981448 0.89018
NM_000141.5(FGFR2):c.2301+1186A>G rs3135814 0.74007
NM_000141.5(FGFR2):c.1987-106A>G rs2981460 0.67642
NM_000141.5(FGFR2):c.-150-388G>A rs3135718 0.54260
NM_000141.5(FGFR2):c.2302-1819T>A rs1799603 0.50482
NM_000141.5(FGFR2):c.2302-1838G>A rs3135817 0.49654
NM_000141.5(FGFR2):c.2057+256C>T rs2288336 0.46149
NM_000141.5(FGFR2):c.1987-99G>A rs2981461 0.45650
NM_000141.5(FGFR2):c.*259C>T rs1047057 0.43446
NM_000141.5(FGFR2):c.2301+1418G>A rs2556537 0.36303
NM_000141.5(FGFR2):c.2301+1829G>A rs1649166 0.32346
NM_000141.5(FGFR2):c.1864-125dup rs4647914 0.28147
NM_000141.5(FGFR2):c.749-112G>A rs2071616 0.25108
NM_000141.5(FGFR2):c.110-320A>G rs2912787 0.24382
NM_000141.5(FGFR2):c.110-179C>G rs2981452 0.20162
NM_000141.5(FGFR2):c.1987-238G>A rs1649199 0.19701
NM_000141.5(FGFR2):c.2302-1820A>T rs11598152 0.18425
NM_000141.5(FGFR2):c.1864-43del rs111564057 0.17733
NM_000141.5(FGFR2):c.624+139A>G rs3135745 0.14394
NM_000141.5(FGFR2):c.624+140T>C rs3135746 0.14357
NM_000141.5(FGFR2):c.2302-1826A>T rs11598153 0.12144
NM_000141.5(FGFR2):c.454+54T>C rs2303568 0.11730
NM_000141.5(FGFR2):c.557T>C (p.Met186Thr) rs755793 0.10553
NM_000141.5(FGFR2):c.455-315T>A rs3135743 0.10507
NM_000141.5(FGFR2):c.1288-161G>A rs3135772 0.10224
NC_000010.11:g.121598656C>T rs4478918 0.09309
NM_000141.5(FGFR2):c.376+213A>T rs7895493 0.07892
NC_000010.11:g.121598582C>G rs41301039 0.04689
NM_000141.5(FGFR2):c.-150-522C>T rs3135717 0.04383
NM_000141.5(FGFR2):c.2195+232G>A rs3135807 0.03826
NM_000141.5(FGFR2):c.2301+1596C>T rs3135816 0.03763
NM_000141.5(FGFR2):c.2196-346dup rs4647920 0.03411
NM_000141.5(FGFR2):c.2196-350G>A rs4647919 0.03297
NM_000141.5(FGFR2):c.1941C>T (p.Leu647=) rs35337478 0.02240
NM_000141.5(FGFR2):c.110-26G>A rs3135733 0.02174
NM_000141.5(FGFR2):c.376+63G>A rs3135734 0.02173
NM_000141.5(FGFR2):c.1864-17T>G rs3135802 0.02120
NM_000141.5(FGFR2):c.2301+1823G>A rs57571942 0.02039
NM_000141.5(FGFR2):c.1561+333G>A rs3135785 0.01896
NM_000141.5(FGFR2):c.1085-222G>A rs41295565 0.01854
NM_000141.5(FGFR2):c.*469G>A rs41294351 0.01826
NM_000141.5(FGFR2):c.-458C>A rs41301043 0.01688
NM_000141.5(FGFR2):c.1288-23G>C rs3135774 0.01572
NM_000141.5(FGFR2):c.455-219C>T rs184026051 0.01446
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.1539C>T (p.Thr513=) rs74160617 0.00234
NM_000141.5(FGFR2):c.-46G>A rs201606812 0.00193
NM_000141.5(FGFR2):c.2001C>G (p.Val667=) rs61731218 0.00187
NM_000141.5(FGFR2):c.1673-12C>T rs41293763 0.00186
NM_000141.5(FGFR2):c.*111G>A rs574474794 0.00164
NM_000141.5(FGFR2):c.454+14C>T rs112142377 0.00152
NM_000141.5(FGFR2):c.23T>G (p.Ile8Ser) rs147307031 0.00107
NM_000141.5(FGFR2):c.34G>A (p.Val12Met) rs143978938 0.00043
NM_000141.5(FGFR2):c.1085-13A>T rs41295573 0.00024
NM_000141.5(FGFR2):c.1548G>A (p.Val516=) rs200522893 0.00006
GRCh37/hg19 10q26.13(chr10:123343892-123348355)x1
NM_000141.5(FGFR2):c.2057+114_2057+135del rs3214540
NM_000141.5(FGFR2):c.2195+75G>A rs1613776
NM_000141.5(FGFR2):c.2301+1196G>A
NM_000141.5(FGFR2):c.2301+1319C>T
NM_000141.5(FGFR2):c.2301+1405G>A
NM_000141.5(FGFR2):c.2301+1756G>A
NM_000141.5(FGFR2):c.2301+494C>T
NM_000141.5(FGFR2):c.2302-1025T>G
NM_000141.5(FGFR2):c.2302-1811_2302-1807dup rs1172844728
NM_000141.5(FGFR2):c.2302-895del
NM_000141.5(FGFR2):c.376+260_376+261dup rs71865754
NM_000141.5(FGFR2):c.376+261dup rs71865754
NM_000141.5(FGFR2):c.939+923C>G rs41295553

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