ClinVar Miner

List of variants in gene FGFR1 reported as likely benign for Kallmann syndrome 2; Pfeiffer syndrome

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Total variants: 5
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HGVS dbSNP
NM_023110.2(FGFR1):c.1285-8C>A rs1235765985
NM_023110.2(FGFR1):c.2106C>T (p.Pro702=) rs777061347
NM_023110.2(FGFR1):c.2186+8C>T rs372639138
NM_023110.2(FGFR1):c.2464C>T (p.Arg822Cys) rs17182463
NM_023110.2(FGFR1):c.471C>G (p.Ser157=) rs376497452

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