List of variants reported as uncertain significance for Kallmann syndrome by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_023110.3(FGFR1):c.1520G>A (p.Arg507His)	rs369356672	0.00009
NM_006080.3(SEMA3A):c.2198G>A (p.Arg733His)	rs318240753	0.00004
NM_001130969.3(NSMF):c.1435A>G (p.Arg479Gly)	rs1174502792	0.00001
NM_033163.5(FGF8):c.157-6C>G	rs2065069146

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