List of variants in gene CTNNA3 reported as benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_013266.4(CTNNA3):c.1603C>T (p.Arg535Cys)	rs41274090	0.01060
NM_013266.4(CTNNA3):c.580-8C>T	rs141983252	0.00170
NM_013266.4(CTNNA3):c.1453A>T (p.Thr485Ser)	rs140913916	0.00130

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