ClinVar Miner

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

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Total variants: 19
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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.-150-522C>T
NM_022970.3(FGFR2):c.-46G>A rs201606812
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.159G>A (p.Ala53=) rs1047102
NM_022970.3(FGFR2):c.1867-125dup
NM_022970.3(FGFR2):c.2060+256C>T
NM_022970.3(FGFR2):c.2304+1186A>G
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.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.749-183G>A

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