List of variants reported as likely pathogenic for Odonto-onycho-dermal dysplasia; SchC6pf-Schulz-Passarge syndrome; Tooth agenesis, selective, 4

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_025216.3(WNT10A):c.682T>A (p.Phe228Ile)	rs121908120	0.01412
NM_025216.3(WNT10A):c.383G>A (p.Arg128Gln)	rs121908121	0.00009
NM_025216.3(WNT10A):c.311G>A (p.Arg104His)	rs374910216	0.00002
NM_025216.3(WNT10A):c.382C>T (p.Arg128Ter)	rs762739726	0.00002
NM_025216.3(WNT10A):c.310C>T (p.Arg104Cys)	rs764658964	0.00001
NM_025216.3(WNT10A):c.403G>A (p.Ala135Thr)	rs1402990329	0.00001
NM_025216.3(WNT10A):c.910A>C (p.Asn304His)	rs1434390821	0.00001
NM_025216.3(WNT10A):c.1247G>A (p.Cys416Tyr)	rs1085308031
NM_025216.3(WNT10A):c.1A>T (p.Met1Leu)	rs1221516695
NM_025216.3(WNT10A):c.322T>C (p.Ser108Pro)	rs1249944381
NM_025216.3(WNT10A):c.376G>A (p.Gly126Ser)
NM_025216.3(WNT10A):c.433G>A (p.Val145Met)	rs543063101
NM_025216.3(WNT10A):c.616C>T (p.Gln206Ter)	rs1060499588
NM_025216.3(WNT10A):c.694del (p.Arg232fs)	rs1575233692
NM_025216.3(WNT10A):c.814C>T (p.Gln272Ter)	rs773036759
NM_025216.3(WNT10A):c.832C>T (p.Gln278Ter)	rs2106018205

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