ClinVar Miner

List of variants in gene FGFR2 reported as likely benign by GeneDx

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Gene type:
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Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_000141.5(FGFR2):c.1439+174T>A rs41295593 0.01608
NM_000141.5(FGFR2):c.1440-231C>T rs3135782 0.01600
NM_000141.5(FGFR2):c.*403A>G rs3135826 0.01590
NM_000141.5(FGFR2):c.1085-256C>A rs4647918 0.01537
NM_000141.5(FGFR2):c.1863+199C>T rs17612814 0.01450
NM_000141.5(FGFR2):c.1673-171C>T rs148685299 0.01385
NM_000141.5(FGFR2):c.2057+220A>T rs3135805 0.01343
NM_000141.5(FGFR2):c.110-54C>T rs3135732 0.01267
NM_000141.5(FGFR2):c.1440-248C>T rs41295621 0.01213
NM_000141.5(FGFR2):c.454+107G>A rs41302307 0.01173
NM_000141.5(FGFR2):c.1439+165A>G rs41295591 0.01109
NM_000141.5(FGFR2):c.1863+246A>G rs41293767 0.00932
NM_000141.5(FGFR2):c.1561+72A>G rs28702981 0.00858
NM_000141.5(FGFR2):c.939+982C>T rs41295555 0.00731
NM_000141.5(FGFR2):c.455-242G>A rs147906363 0.00577
NM_000141.5(FGFR2):c.1987-129T>C rs3135804 0.00564
NM_000141.5(FGFR2):c.2302-219C>A rs3135823 0.00553
NM_000141.5(FGFR2):c.749-27T>C rs41295547 0.00541
NM_000141.5(FGFR2):c.1987-165T>G rs74500478 0.00526
NM_000141.5(FGFR2):c.1987-166A>C rs79305817 0.00526
NM_000141.5(FGFR2):c.1673-273C>T rs181663041 0.00458
NM_000141.5(FGFR2):c.1288-158G>A rs3135773 0.00375
NM_000141.5(FGFR2):c.-150-132G>A rs41301563 0.00374
NM_000141.5(FGFR2):c.1672+336A>G rs527799074 0.00361
NM_000141.5(FGFR2):c.1672+181T>G rs41293747 0.00358
NM_000141.5(FGFR2):c.940-36C>T rs112692991 0.00320
NM_000141.5(FGFR2):c.1572A>G (p.Thr524=) rs74160613 0.00298
NM_000141.5(FGFR2):c.1561+179T>C rs74160616 0.00292
NM_000141.5(FGFR2):c.1439+95A>G rs41295589 0.00277
NM_000141.5(FGFR2):c.-61G>T rs3135721 0.00130
NM_000141.5(FGFR2):c.759T>G (p.Pro253=) rs3135755 0.00057
NM_000141.5(FGFR2):c.34G>A (p.Val12Met) rs143978938 0.00043
NM_000141.5(FGFR2):c.2190C>T (p.Asn730=) rs55637244 0.00040
NM_000141.5(FGFR2):c.789G>A (p.Pro263=) rs138315382 0.00038
NM_000141.5(FGFR2):c.2232C>T (p.Pro744=) rs142639988 0.00035
NM_000141.5(FGFR2):c.1986+7C>T rs199697707 0.00032
NM_000141.5(FGFR2):c.1911C>T (p.Asn637=) rs149008039 0.00026
NM_000141.5(FGFR2):c.263T>C (p.Ile88Thr) rs200369248 0.00022
NM_000141.5(FGFR2):c.989G>A (p.Arg330Gln) rs199757302 0.00011
NM_000141.5(FGFR2):c.942C>T (p.Ala314=) rs201717227 0.00008
NM_000141.5(FGFR2):c.-6G>A rs772427122 0.00006
NM_000141.5(FGFR2):c.1362G>A (p.Thr454=) rs200183009 0.00006
NM_000141.5(FGFR2):c.420G>A (p.Ala140=) rs765024365 0.00006
NM_000141.5(FGFR2):c.306C>T (p.Ser102=) rs368662264 0.00005
NM_000141.5(FGFR2):c.2415C>T (p.Tyr805=) rs558460047 0.00004
NM_000141.5(FGFR2):c.1086G>A (p.Ala362=) rs151250769 0.00003
NM_000141.5(FGFR2):c.1155C>G (p.Val385=) rs531426519 0.00001
NM_000141.5(FGFR2):c.2058-10T>C rs756377540 0.00001
NM_000141.5(FGFR2):c.2283C>T (p.Leu761=) rs753103160 0.00001
NM_000141.5(FGFR2):c.234C>T (p.His78=) rs778093907 0.00001
NM_000141.5(FGFR2):c.377-10T>C rs1253602922 0.00001
NC_000010.11:g.121598531C>T rs753202350
NM_000141.5(FGFR2):c.-151+19G>T rs974988741
NM_000141.5(FGFR2):c.1084+20T>C rs1554928776
NM_000141.5(FGFR2):c.110-195G>C rs529146683
NM_000141.5(FGFR2):c.1287+287GT[5] rs576981699
NM_000141.5(FGFR2):c.1439+185dup rs11365153
NM_000141.5(FGFR2):c.2328C>T (p.Leu776=) rs148478597
NM_000141.5(FGFR2):c.376+259_376+261dup rs71865754
NM_000141.5(FGFR2):c.376+261del rs71865754
NM_000141.5(FGFR2):c.624+70dup rs199542453

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