ClinVar Miner

List of variants reported as likely pathogenic for Kallmann syndrome 6

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Total variants: 3
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NM_033163.4(FGF8):c.237C>G (p.Leu79=) rs606231408
NM_033163.4(FGF8):c.451G>A (p.Gly151Ser) rs606231407
NM_033164.4(FGF8):c.595_596dup (p.His200fs) rs1554834303

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