List of variants in gene ADAMTS10 reported as likely pathogenic for bone disorder

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

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_030957.4(ADAMTS10):c.1179G>C (p.Glu393Asp)	rs782097535
NM_030957.4(ADAMTS10):c.1183G>A (p.Gly395Arg)	rs781920954
NM_030957.4(ADAMTS10):c.1219A>G (p.Asn407Asp)	rs2512622286
NM_030957.4(ADAMTS10):c.1462C>A (p.Arg488Ser)	rs782720992
NM_030957.4(ADAMTS10):c.1893C>A (p.Tyr631Ter)	rs1235872718
NM_030957.4(ADAMTS10):c.2720G>A (p.Arg907His)	rs2512575769
NM_030957.4(ADAMTS10):c.2986C>T (p.Arg996Cys)	rs1159059721
NM_030957.4(ADAMTS10):c.3083T>G (p.Val1028Gly)	rs1339572177
NM_030957.4(ADAMTS10):c.698G>A (p.Arg233Gln)	rs1555741462
NM_030957.4(ADAMTS10):c.726_727del (p.Glu242fs)	rs2512639575

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