ClinVar Miner

List of variants in gene combination FGFR1, LOC102723716 reported as benign for hypogonadotropic hypogonadism 2 with or without anosmia

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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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.*723G>C rs17182477 0.00220
NM_023110.3(FGFR1):c.*1498C>T rs17182484 0.00141
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.*963C>T rs567128409 0.00015
NM_023110.3(FGFR1):c.*2434C>T rs565758830 0.00007
NM_023110.3(FGFR1):c.*1052C>T rs17176088

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