List of variants in gene AXIN2 reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_004655.4(AXIN2):c.2272G>A (p.Ala758Thr)	rs145007501	0.00179
NM_004655.4(AXIN2):c.1807G>C (p.Ala603Pro)	rs145353986	0.00128
NM_004655.4(AXIN2):c.2428G>A (p.Asp810Asn)	rs140344858	0.00123
NM_004655.4(AXIN2):c.1168A>G (p.Ser390Gly)	rs139871607	0.00075
NM_004655.4(AXIN2):c.1250C>T (p.Ala417Val)	rs201460658	0.00064
NM_004655.4(AXIN2):c.2285G>A (p.Ser762Asn)	rs117688560	0.00064
NM_004655.4(AXIN2):c.1491C>T (p.Cys497=)	rs150292240	0.00024
NM_004655.4(AXIN2):c.1975C>T (p.Arg659Trp)	rs142670753	0.00014
NM_004655.4(AXIN2):c.2478G>T (p.Thr826=)	rs148159432	0.00006
NM_004655.4(AXIN2):c.623C>T (p.Ala208Val)	rs201531372	0.00006
NM_004655.4(AXIN2):c.1665C>T (p.Cys555=)	rs562421443	0.00003
NM_004655.4(AXIN2):c.1827C>T (p.Pro609=)	rs747605090	0.00002
NM_004655.4(AXIN2):c.711C>T (p.Ala237=)	rs768230770	0.00002
NM_004655.4(AXIN2):c.2499C>A (p.Gly833=)	rs772461187	0.00001
NM_004655.4(AXIN2):c.1338C>A (p.Val446=)	rs369864600
NM_004655.4(AXIN2):c.1608G>A (p.Thr536=)	rs1403070766
NM_004655.4(AXIN2):c.1821G>A (p.Gln607=)	rs1242108165

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