ClinVar Miner

List of variants in gene FGFR1, LOC102723716 studied for Hypogonadotropic hypogonadism 2 with or without anosmia

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Gene type:
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Total variants: 46
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HGVS dbSNP gnomAD frequency
NM_023110.3(FGFR1):c.*1632A>G rs13317 0.22837
NM_023110.3(FGFR1):c.*2099T>G rs16887356 0.00560
NM_023110.3(FGFR1):c.*2188T>C rs146463691 0.00411
NM_023110.3(FGFR1):c.*994T>C rs17176081 0.00273
NM_023110.3(FGFR1):c.*906A>T rs139347382 0.00249
NM_023110.3(FGFR1):c.*723G>C rs17182477 0.00220
NM_023110.3(FGFR1):c.*1026T>C rs542417198 0.00214
NM_023110.3(FGFR1):c.*1439T>C rs11990198 0.00186
NM_023110.3(FGFR1):c.*1498C>T rs17182484 0.00141
NM_023110.3(FGFR1):c.*1446A>C rs578094209 0.00081
NM_023110.3(FGFR1):c.*1770G>A rs183394116 0.00072
NM_023110.3(FGFR1):c.*1211G>T rs185104092 0.00038
NM_023110.3(FGFR1):c.*1055C>T rs761124911 0.00035
NM_023110.3(FGFR1):c.*1822A>C rs570038633 0.00031
NM_023110.3(FGFR1):c.*2057C>T rs556829066 0.00031
NM_023110.3(FGFR1):c.*2391A>G rs185729862 0.00024
NM_023110.3(FGFR1):c.*1711G>A rs567642271 0.00021
NM_023110.3(FGFR1):c.*963C>T rs567128409 0.00015
NM_023110.3(FGFR1):c.*2407C>T rs758524862 0.00010
NM_023110.3(FGFR1):c.*957C>T rs941835357 0.00009
NM_023110.3(FGFR1):c.*2434C>T rs565758830 0.00007
NM_023110.3(FGFR1):c.*1286C>T rs886062909 0.00003
NM_023110.3(FGFR1):c.*1560C>T rs761096092 0.00003
NM_023110.3(FGFR1):c.*1965G>A rs886062907 0.00003
NM_023110.3(FGFR1):c.*2408C>T rs1004230937 0.00003
NM_023110.3(FGFR1):c.*762A>G rs886062914 0.00003
NM_023110.3(FGFR1):c.*802C>T rs938792635 0.00003
NM_023110.3(FGFR1):c.*991G>A rs866647792 0.00003
NM_023110.3(FGFR1):c.*913G>A rs886062912 0.00002
NM_023110.3(FGFR1):c.*1086A>T rs1287148499 0.00001
NM_023110.3(FGFR1):c.*1149G>A rs923197183 0.00001
NM_023110.3(FGFR1):c.*2445A>G rs1261528641 0.00001
NM_023110.3(FGFR1):c.*928G>A rs1814772534 0.00001
NM_023110.3(FGFR1):c.*1052C>T rs17176088
NM_023110.3(FGFR1):c.*1111C>T rs867360704
NM_023110.3(FGFR1):c.*1124C>G rs561923573
NM_023110.3(FGFR1):c.*1144G>A rs886062911
NM_023110.3(FGFR1):c.*1218T>C rs886062910
NM_023110.3(FGFR1):c.*1616T>G rs886062908
NM_023110.3(FGFR1):c.*1676G>A rs763761019
NM_023110.3(FGFR1):c.*1723C>T rs1200256665
NM_023110.3(FGFR1):c.*1823G>A rs1814497706
NM_023110.3(FGFR1):c.*1982A>C rs536000259
NM_023110.3(FGFR1):c.*819T>G rs1814814648
NM_023110.3(FGFR1):c.*845T>C rs886062913
NM_023110.3(FGFR1):c.*958G>A rs537880800

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