ClinVar Miner

List of variants in gene WNT10B reported as likely pathogenic for bone development disease

Included ClinVar conditions (614):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_003394.4(WNT10B):c.676C>T (p.Arg226Ter) rs763991433 0.00001
NM_003394.4(WNT10B):c.115G>T (p.Glu39Ter)
NM_003394.4(WNT10B):c.257A>C (p.Gln86Pro) rs1592252556
NM_003394.4(WNT10B):c.338-1G>C rs1163162816
NM_003394.4(WNT10B):c.53T>A (p.Leu18Gln)
NM_003394.4(WNT10B):c.746G>T (p.Cys249Phe)
NM_003394.4(WNT10B):c.949T>A (p.Phe317Ile)

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