List of variants in gene CTNNB1, LOC126806659 studied for Medulloblastoma; Pilomatrixoma; Ovarian neoplasm; Severe intellectual disability-progressive spastic diplegia syndrome; Hepatocellular carcinoma; Colorectal cancer; Exudative vitreoretinopathy 7

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001904.4(CTNNB1):c.1683+17A>G	rs2276826	0.00068
NM_001904.4(CTNNB1):c.1420C>T (p.Arg474Ter)	rs1553631860
NM_001904.4(CTNNB1):c.1543C>T (p.Arg515Ter)	rs397514554
NM_001904.4(CTNNB1):c.1571A>G (p.His524Arg)	rs1376864427

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