ClinVar Miner

List of variants in gene FGFR3 reported as likely benign by GeneDx

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Gene type:
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Total variants: 19
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HGVS dbSNP
NM_000142.4(FGFR3):c.-102-9C>T rs1035034826
NM_000142.4(FGFR3):c.1534+14G>T rs374221323
NM_000142.4(FGFR3):c.1645+17C>T rs765768657
NM_000142.4(FGFR3):c.379+18G>A rs775716751
NM_000142.4(FGFR3):c.615+11C>T rs780810190
NM_000142.4(FGFR3):c.615+20T>C rs1374050784
NM_000142.4(FGFR3):c.616-18G>C rs372940259
NM_000142.4(FGFR3):c.739+16C>T rs757999433
NM_000142.4(FGFR3):c.740-17G>A rs371424896
NM_000142.5(FGFR3):c.1205C>G (p.Pro402Arg) rs752194597
NM_000142.5(FGFR3):c.1576A>G (p.Met526Val) rs766053734
NM_000142.5(FGFR3):c.201T>C (p.Gly67=) rs752621056
NM_000142.5(FGFR3):c.2088C>T (p.Pro696=) rs142884145
NM_000142.5(FGFR3):c.21C>T (p.Ala7=) rs779195790
NM_000142.5(FGFR3):c.2249G>T (p.Arg750Leu) rs762888506
NM_000142.5(FGFR3):c.2270C>G (p.Thr757Ser) rs748763892
NM_000142.5(FGFR3):c.573C>T (p.Asn191=) rs377492283
NM_000142.5(FGFR3):c.666C>T (p.Asp222=) rs201081464
NM_000142.5(FGFR3):c.808G>A (p.Asp270Asn) rs780147591

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