C1835492[trait identifier] AND "MGZ Medical Genetics Center"[submitter - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 4461	NM_025216.3(WNT10A):c.321C>A (p.Cys107Ter)	WNT10A (C107*)	Single nucleotide variant (nonsense)	not provided +6 more	GPathogenic
Select item 372548	NM_025216.3(WNT10A):c.337C>T (p.Arg113Cys)	WNT10A (R113C)	Single nucleotide variant (missense variant)	WNT10A-related disorder +3 more	GConflicting classifications of pathogenicity
Select item 464182	NM_025216.3(WNT10A):c.433G>A (p.Val145Met)	WNT10A (V145M)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 4 +1 more	GPathogenic/Likely pathogenic
Select item 4462	NM_025216.3(WNT10A):c.682T>A (p.Phe228Ile)	WNT10A (F228I)	Single nucleotide variant (missense variant)	SchC6pf-Schulz-Passarge syndrome +7 more	GConflicting classifications of pathogenicity
Select item 639357	NM_025216.3(WNT10A):c.694del (p.Arg232fs)	WNT10A (R232fs)	Deletion (frameshift variant)	not provided +3 more	GPathogenic/Likely pathogenic
Select item 841749	NM_025216.3(WNT10A):c.814C>T (p.Gln272Ter)	WNT10A (Q272*)	Single nucleotide variant (nonsense)	not provided +3 more	GPathogenic/Likely pathogenic

ClinVar