ClinVar Miner

List of variants in gene FGFR3 reported as benign by GeneDx

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Gene type:
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Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_000142.5(FGFR3):c.-102-3T>C rs10023340 0.99671
NM_000142.5(FGFR3):c.931-123G>A rs3135883 0.91705
NM_000142.5(FGFR3):c.930+625G>A rs3135878 0.82366
NM_000142.5(FGFR3):c.-103+129C>A rs4450996 0.59323
NM_000142.5(FGFR3):c.616-40T>C rs2305183 0.21932
NM_000142.5(FGFR3):c.882T>C (p.Asn294=) rs2234909 0.20412
NM_000142.5(FGFR3):c.930+72C>G rs2305184 0.19439
NM_000142.5(FGFR3):c.109+309C>T rs3135834 0.10213
NM_000142.5(FGFR3):c.445+3A>G rs3135868 0.09950
NM_000142.5(FGFR3):c.1267-32C>T rs3135890 0.09901
NM_000142.5(FGFR3):c.603T>C (p.Ile201=) rs2305181 0.09854
NM_000142.5(FGFR3):c.445+158T>C rs3135869 0.08952
NM_000142.5(FGFR3):c.1953= (p.Thr651=) rs7688609 0.04271
NM_000142.5(FGFR3):c.*184C>T rs3135901 0.04173
NM_000142.5(FGFR3):c.417C>T (p.Asp139=) rs3135867 0.03551
NM_000142.5(FGFR3):c.1075+236T>C rs3135888 0.03378
NM_000142.5(FGFR3):c.588C>T (p.Arg196=) rs2305180 0.03125
NM_000142.5(FGFR3):c.930+174T>C rs3135874 0.02902
NM_000142.5(FGFR3):c.109+174T>C rs17884005 0.02494
NM_000142.5(FGFR3):c.*36A>G rs3135900 0.02388
NM_000142.5(FGFR3):c.615+8C>G rs17878375 0.02283
NM_000142.5(FGFR3):c.1076-17C>T rs17881967 0.02051
NM_000142.5(FGFR3):c.348C>T (p.Arg116=) rs2305179 0.01752
NM_000142.5(FGFR3):c.1959+22G>A rs3135898 0.01743
NM_000142.5(FGFR3):c.1075+5C>T rs3135885 0.01659
NM_000142.5(FGFR3):c.1345C>T (p.Pro449Ser) rs61735104 0.00867
NM_000142.5(FGFR3):c.654G>C (p.Val218=) rs147769045 0.00703
NM_000142.5(FGFR3):c.1076-13C>T rs114754024 0.00661
NM_000142.5(FGFR3):c.1645+15G>A rs192433202 0.00533
NM_000142.5(FGFR3):c.616-15C>T rs17883683 0.00494
NM_000142.5(FGFR3):c.663G>A (p.Ser221=) rs114421370 0.00485
NM_000142.5(FGFR3):c.1150T>C (p.Phe384Leu) rs17881656 0.00342
NM_000142.5(FGFR3):c.1535-8G>T rs111460786 0.00332
NM_000142.5(FGFR3):c.1014C>T (p.Thr338=) rs4647928 0.00328
NM_000142.5(FGFR3):c.1076-16G>A rs3135889 0.00296
NM_000142.5(FGFR3):c.393G>A (p.Ser131=) rs55662109 0.00292
NM_000142.5(FGFR3):c.2205C>G (p.Pro735=) rs145020302 0.00287
NM_000142.5(FGFR3):c.*5C>G rs17879364 0.00201
NM_000142.5(FGFR3):c.1535-20G>A rs113557371 0.00174
NM_000142.5(FGFR3):c.169G>A (p.Val57Met) rs61735064 0.00163
NM_000142.5(FGFR3):c.1413-16C>G rs201702411 0.00114
NM_000142.5(FGFR3):c.1497C>T (p.Ala499=) rs140594137 0.00106
NM_000142.5(FGFR3):c.2043G>A (p.Gly681=) rs17883356 0.00101
NM_000142.5(FGFR3):c.193G>A (p.Gly65Arg) rs2305178 0.00097
NM_000142.5(FGFR3):c.990C>T (p.Thr330=) rs2305185 0.00097
NM_000142.5(FGFR3):c.2149G>A (p.Ala717Thr) rs17882190 0.00095
NM_000142.5(FGFR3):c.1349C>T (p.Thr450Met) rs56240927 0.00083
NM_000142.5(FGFR3):c.1923C>T (p.Asp641=) rs148104605 0.00081
NM_000142.5(FGFR3):c.1671C>T (p.Tyr557=) rs370408732 0.00057
NM_000142.5(FGFR3):c.252G>A (p.Ser84=) rs367973461 0.00039
NM_000142.5(FGFR3):c.1960-13C>T rs377604726 0.00011
NM_000142.5(FGFR3):c.1285G>A (p.Ala429Thr) rs182935140 0.00008
NM_000142.5(FGFR3):c.1935C>T (p.Leu645=) rs104886006 0.00002
NM_000142.5(FGFR3):c.*140TG[8] rs34562534
NM_000142.5(FGFR3):c.-102-18_-102-11del rs1452696194
NM_000142.5(FGFR3):c.-103+141C>T rs17879199
NM_000142.5(FGFR3):c.1075+30G>C rs3135886
NM_000142.5(FGFR3):c.1076-34del rs4647926
NM_000142.5(FGFR3):c.1076-34dup rs4647926
NM_000142.5(FGFR3):c.1412+138G>C rs4865476
NM_000142.5(FGFR3):c.1413-29A>G rs3135894
NM_000142.5(FGFR3):c.1647G>T (p.Gly549=) rs3135897
NM_000142.5(FGFR3):c.930+218G>A rs3135875

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