List of variants reported as likely pathogenic for Tooth agenesis, selective, 4

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Total variants: 12

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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.337C>T (p.Arg113Cys)	rs141074983	0.00080
NM_025216.3(WNT10A):c.383G>A (p.Arg128Gln)	rs121908121	0.00009
NM_025216.3(WNT10A):c.1070C>T (p.Thr357Ile)	rs750190755	0.00001
NM_025216.3(WNT10A):c.627G>A (p.Trp209Ter)	rs1306584103	0.00001
NM_025216.3(WNT10A):c.889G>A (p.Ala297Thr)	rs530717943	0.00001
NM_025216.3(WNT10A):c.1036del (p.Cys346fs)	rs761182689
NM_025216.3(WNT10A):c.353A>G (p.Tyr118Cys)	rs1559412676
NM_025216.3(WNT10A):c.354T>G (p.Tyr118Ter)
NM_025216.3(WNT10A):c.521T>C (p.Leu174Pro)	rs777307167
NM_025216.3(WNT10A):c.812G>A (p.Cys271Tyr)	rs2469036249
NM_025216.3(WNT10A):c.814C>T (p.Gln272Ter)	rs773036759

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