List of variants in gene TCF12 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_207037.2(TCF12):c.1036-6G>A
NM_207037.2(TCF12):c.1606del (p.Thr536fs)	rs1597730335
NM_207037.2(TCF12):c.1746-8T>G
NM_207037.2(TCF12):c.1769del (p.Asp589_Leu590insTer)	rs1597816045
NM_207037.2(TCF12):c.1807C>T (p.Arg603Trp)	rs1191340189
NM_207037.2(TCF12):c.1808G>A (p.Arg603Gln)	rs1349009265
NM_207037.2(TCF12):c.1837C>T (p.Arg613Cys)	rs1414251456
NM_207037.2(TCF12):c.1838G>A (p.Arg613His)
NM_207037.2(TCF12):c.268C>T (p.Arg90Ter)	rs747222651
NM_207037.2(TCF12):c.325+2T>C
NM_207037.2(TCF12):c.655del (p.Ser219fs)
NM_207037.2(TCF12):c.778_779del (p.Met260fs)	rs2059175292
NM_207037.2(TCF12):c.784C>T (p.Gln262Ter)

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