List of variants reported as uncertain significance for TCF12-related craniosynostosis

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_207037.2(TCF12):c.1720A>C (p.Lys574Gln)	rs1057518720	0.00001
NM_207037.2(TCF12):c.*646T>G	rs1204777319
NM_207037.2(TCF12):c.1035+4660C>T	rs2151950851
NM_207037.2(TCF12):c.1808G>A (p.Arg603Gln)	rs1349009265
NM_207037.2(TCF12):c.1837C>T (p.Arg613Cys)	rs1414251456
NM_207037.2(TCF12):c.1952T>G (p.Ile651Ser)
NM_207037.2(TCF12):c.1991del (p.Asn664fs)
NM_207037.2(TCF12):c.2068C>T (p.Pro690Ser)	rs2061739586
NM_207037.2(TCF12):c.801C>T (p.Gly267=)	rs2059176608

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