List of variants studied for Kallmann syndrome by Revvity Omics, Revvity

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_144773.4(PROKR2):c.518T>G (p.Leu173Arg)	rs74315416	0.00220
NM_033163.5(FGF8):c.77C>T (p.Pro26Leu)	rs137852660	0.00079
NM_001059.3(TACR3):c.824G>A (p.Trp275Ter)	rs144292455	0.00039
NM_033163.5(FGF8):c.451G>A (p.Gly151Ser)	rs606231407	0.00002
NM_144773.4(PROKR2):c.691G>A (p.Glu231Lys)	rs538606142	0.00001
NM_000216.4(ANOS1):c.1704C>A (p.His568Gln)
NM_001130969.3(NSMF):c.194C>A (p.Pro65His)
NM_144773.4(PROKR2):c.201C>A (p.Cys67Ter)
NM_144773.4(PROKR2):c.58del (p.His20fs)	rs587777834
NM_144773.4(PROKR2):c.937A>G (p.Thr313Ala)
NM_198391.3(FLRT3):c.1727C>T (p.Ala576Val)

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