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

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_003394.4(WNT10B):c.458_461dup (p.Asp155fs)	rs763548858	0.00001
NM_003394.4(WNT10B):c.994C>T (p.Arg332Trp)	rs121918349	0.00001
NM_003394.4(WNT10B):c.117_136del (p.Glu39fs)	rs2137615101
NM_003394.4(WNT10B):c.338-1G>C	rs1163162816
NM_003394.4(WNT10B):c.499_500del (p.Leu167fs)	rs2137612860
NM_003394.4(WNT10B):c.689ACA[2] (p.Asn232del)	rs776938956
NM_003394.4(WNT10B):c.741del (p.Lys246_Cys247insTer)	rs2137611223
NM_003394.4(WNT10B):c.817del (p.Ala273fs)
NM_003394.4(WNT10B):c.817dup (p.Ala273fs)

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