List of variants in gene AXIN2 reported as 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: 26

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HGVS	dbSNP	gnomAD frequency
NM_004655.4(AXIN2):c.1365A>G (p.Pro455=)	rs9915936	0.90382
NM_004655.4(AXIN2):c.1386C>T (p.Pro462=)	rs1133683	0.52439
NM_004655.4(AXIN2):c.148C>T (p.Pro50Ser)	rs2240308	0.39067
NM_004655.4(AXIN2):c.1712+19G>T	rs7219582	0.14767
NM_004655.4(AXIN2):c.1060-17C>T	rs35399989	0.13976
NM_004655.4(AXIN2):c.2062C>T (p.Leu688=)	rs35415678	0.11118
NM_004655.4(AXIN2):c.956+16A>G	rs35285779	0.08430
NM_004655.4(AXIN2):c.432T>C (p.Ile144=)	rs2240307	0.04207
NM_004655.4(AXIN2):c.1383C>T (p.Ser461=)	rs9914661	0.01367
NM_004655.4(AXIN2):c.1615G>A (p.Val539Met)	rs9913621	0.01361
NM_004655.4(AXIN2):c.1573C>G (p.Pro525Ala)	rs73346297	0.00930
NM_004655.4(AXIN2):c.2282C>A (p.Ala761Asp)	rs79732150	0.00649
NM_004655.4(AXIN2):c.2109G>A (p.Arg703=)	rs116525755	0.00396
NM_004655.4(AXIN2):c.1410C>T (p.His470=)	rs149483825	0.00394
NM_004655.4(AXIN2):c.1952C>T (p.Ser651Leu)	rs74006838	0.00128
NM_004655.4(AXIN2):c.2051C>T (p.Ala684Val)	rs138287857	0.00112
NM_004655.4(AXIN2):c.1101C>T (p.Pro367=)	rs141697521	0.00094
NM_004655.4(AXIN2):c.1985T>C (p.Leu662Pro)	rs142476324	0.00084
NM_004655.4(AXIN2):c.270C>T (p.Asp90=)	rs141655687	0.00076
NM_004655.4(AXIN2):c.2052G>A (p.Ala684=)	rs200573256	0.00046
NM_004655.4(AXIN2):c.1685C>T (p.Pro562Leu)	rs149764887	0.00031
NM_004655.4(AXIN2):c.1181G>A (p.Arg394His)	rs200899695	0.00010
NM_004655.4(AXIN2):c.1671C>T (p.Ser557=)	rs763146338	0.00001
NM_004655.4(AXIN2):c.1235A>G (p.Asn412Ser)	rs115931022
NM_004655.4(AXIN2):c.2013_2024del (p.Thr672_Arg675del)	rs151279728
NM_004655.4(AXIN2):c.2124G>C (p.Ser708=)	rs143243661

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