ClinVar Miner

List of variants reported as likely pathogenic for odonto-onycho-dermal dysplasia

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_025216.3(WNT10A):c.383G>A (p.Arg128Gln) rs121908121 0.00007
NM_025216.3(WNT10A):c.391G>A (p.Ala131Thr) rs372993798 0.00004
NM_025216.3(WNT10A):c.382C>T (p.Arg128Ter) rs762739726 0.00002
NM_025216.3(WNT10A):c.1028C>T (p.Pro343Leu) rs1944675271 0.00001
NM_025216.3(WNT10A):c.310C>T (p.Arg104Cys) rs764658964 0.00001
NM_025216.3(WNT10A):c.-17_13del (p.Met1_His5del) rs746813123
NM_025216.3(WNT10A):c.1066G>A (p.Gly356Ser)
NM_025216.3(WNT10A):c.1079G>C (p.Arg360Pro) rs893127185
NM_025216.3(WNT10A):c.113+1G>A
NM_025216.3(WNT10A):c.274G>A (p.Ala92Thr)
NM_025216.3(WNT10A):c.318C>G (p.Asn106Lys) rs1283426045
NM_025216.3(WNT10A):c.322T>C (p.Ser108Pro) rs1249944381
NM_025216.3(WNT10A):c.3G>A (p.Met1Ile)
NM_025216.3(WNT10A):c.433G>A (p.Val145Met) rs543063101
NM_025216.3(WNT10A):c.521T>C (p.Leu174Pro)
NM_025216.3(WNT10A):c.616C>T (p.Gln206Ter) rs1060499588
NM_025216.3(WNT10A):c.662G>T (p.Gly221Val)
NM_025216.3(WNT10A):c.694del (p.Arg232fs) rs1575233692
NM_025216.3(WNT10A):c.814C>T (p.Gln272Ter) rs773036759
NM_025216.3(WNT10A):c.949del (p.Ala317fs) rs775990266

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