List of variants in gene combination CTNNB1, LOC126806658 reported as likely pathogenic for bone benign neoplasm

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001904.4(CTNNB1):c.100G>A (p.Gly34Arg)	rs121913399
NM_001904.4(CTNNB1):c.100G>C (p.Gly34Arg)	rs121913399
NM_001904.4(CTNNB1):c.101G>T (p.Gly34Val)	rs28931589
NM_001904.4(CTNNB1):c.94G>T (p.Asp32Tyr)	rs28931588

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