ClinVar Miner

List of variants in gene FGFR2 reported as benign

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Total variants: 36
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HGVS dbSNP
GRCh37/hg19 10q26.13(chr10:123343892-123348355)x1
NM_022970.3(FGFR2):c.*259C>T rs1047057
NM_022970.3(FGFR2):c.*469G>A rs41294351
NM_022970.3(FGFR2):c.-150-522C>T
NM_022970.3(FGFR2):c.-157A>G rs41258305
NM_022970.3(FGFR2):c.-236G>A rs1047111
NM_022970.3(FGFR2):c.-236G>C rs1047111
NM_022970.3(FGFR2):c.-318G>C rs41301547
NM_022970.3(FGFR2):c.-46G>A rs201606812
NM_022970.3(FGFR2):c.1087+1249A>G rs1443966407
NM_022970.3(FGFR2):c.109+10T>G rs3135722
NM_022970.3(FGFR2):c.1291-161G>A
NM_022970.3(FGFR2):c.1291-23G>C
NM_022970.3(FGFR2):c.1575A>G (p.Thr525=) rs74160613
NM_022970.3(FGFR2):c.159G>A (p.Ala53=) rs1047102
NM_022970.3(FGFR2):c.170C>T (p.Ser57Leu) rs56226109
NM_022970.3(FGFR2):c.17G>C (p.Arg6Pro) rs3750819
NM_022970.3(FGFR2):c.1867-125dup
NM_022970.3(FGFR2):c.1867-17T>G rs3135802
NM_022970.3(FGFR2):c.1944C>T (p.Leu648=) rs35337478
NM_022970.3(FGFR2):c.2004C>G (p.Val668=) rs61731218
NM_022970.3(FGFR2):c.2060+256C>T
NM_022970.3(FGFR2):c.2304+1186A>G
NM_022970.3(FGFR2):c.2304+15C>T rs2278202
NM_022970.3(FGFR2):c.2304+1716A>G
NM_022970.3(FGFR2):c.2304+1829G>A
NM_022970.3(FGFR2):c.2305-1838G>A
NM_022970.3(FGFR2):c.23T>G (p.Ile8Ser) rs147307031
NM_022970.3(FGFR2):c.294G>A (p.Thr98=) rs1047101
NM_022970.3(FGFR2):c.455-315T>A
NM_022970.3(FGFR2):c.557T>C (p.Met186Thr) rs755793
NM_022970.3(FGFR2):c.624+139A>G
NM_022970.3(FGFR2):c.624+140T>C
NM_022970.3(FGFR2):c.696A>G (p.Val232=) rs1047100
NM_022970.3(FGFR2):c.749-183G>A
NM_022970.3(FGFR2):c.755C>T (p.Ser252Leu) rs79184941

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