WNT3A

Wnt family member 3A

Summary

The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It encodes a protein which shows 96% amino acid identity to mouse Wnt3A protein, and 84% to human WNT3 protein, another WNT gene product. This gene is clustered with WNT14 gene, another family member, in chromosome 1q42 region. [provided by RefSeq, Jul 2008]

Known Variants126 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs708113	1:228,192,753	T/A	regulatory region variant	—
rs1369668727	1:228,194,840	T/C	—	uncertain significance
rs1217224419	1:228,194,841	C/T	—	likely benign
rs2528130723	1:228,194,854	C/T	—	uncertain significance
rs772366201	1:228,194,856	C/G	—	likely benign
rs2528130768	1:228,194,879	T/C	—	uncertain significance
rs771033634	1:228,194,885	G/A	—	uncertain significance
rs564795189	1:228,194,892	G/A	—	likely benign
rs1214937775	1:228,194,916	C/G	—	likely benign
rs708119	1:228,203,268	C/G	regulatory region variant	—
rs1745416	1:228,204,497	G/A	intron variant	—
rs541407192	1:228,210,349	C/T	—	benign
rs368553652	1:228,210,350	G/A	—	likely benign
rs376115959	1:228,210,371	G/A	—	likely benign
rs1329090456	1:228,210,384	C/T	—	uncertain significance
rs1558286309	1:228,210,398	C/A	—	likely benign
rs767062258	1:228,210,407	G/A	—	likely benign
rs145797401	1:228,210,448	A/G	—	uncertain significance
rs199976080	1:228,210,474	G/A	—	uncertain significance
rs779941062	1:228,210,482	C/G	—	uncertain significance
rs2528151467	1:228,210,488	C/A	—	likely benign
rs774063132	1:228,210,492	G/T	—	uncertain significance
rs548478697	1:228,210,498	G/A	—	uncertain significance
rs760074981	1:228,210,511	T/G	—	uncertain significance
rs1346108878	1:228,210,522	G/T	—	uncertain significance
rs367839893	1:228,210,524	G/A	—	likely benign
rs1213331058	1:228,210,539	C/A	—	uncertain significance
rs753280205	1:228,210,540	C/T	—	uncertain significance
rs142644449	1:228,210,541	G/A	—	uncertain significance
rs764558716	1:228,210,542	C/T	—	likely benign
rs371989231	1:228,210,543	G/A	—	uncertain significance
rs756167532	1:228,210,548	C/T	—	likely benign
rs749224268	1:228,210,550	G/A	—	uncertain significance
rs375328733	1:228,210,566	C/T	—	likely benign
rs572229142	1:228,210,567	G/A	—	uncertain significance
rs201572822	1:228,210,572	C/T	—	likely benign
rs201274685	1:228,210,573	G/A	—	benign
rs760328956	1:228,210,580	T/A	—	uncertain significance
rs776215625	1:228,210,585	A/G	—	uncertain significance
rs2102765307	1:228,210,591	G/A	—	uncertain significance
rs767871879	1:228,210,596	C/T	—	likely benign
rs754980378	1:228,210,626	G/A	—	likely benign
rs374518471	1:228,210,627	G/T	—	likely benign
rs2030756326	1:228,210,628	G/A	—	likely benign
rs992064069	1:228,225,337	C/G	—	—
rs760949821	1:228,238,338	A/G	—	likely benign
rs2031524631	1:228,238,346	T/A	—	likely benign
rs373278590	1:228,238,370	G/A	—	likely benign
rs745466989	1:228,238,388	T/G	—	uncertain significance
rs151253698	1:228,238,397	C/T	—	likely benign
rs774995569	1:228,238,398	G/A	—	uncertain significance
rs201868384	1:228,238,415	G/A	—	benign
rs370854032	1:228,238,420	G/A	—	uncertain significance
rs2464480817	1:228,238,427	T/C	—	likely benign
rs765238501	1:228,238,439	G/A	—	likely benign
rs752764092	1:228,238,442	C/T	—	likely benign
rs61743220	1:228,238,443	G/A	—	benign
rs148616293	1:228,238,465	G/A	—	uncertain significance
rs988241577	1:228,238,480	C/T	—	uncertain significance
rs2464481134	1:228,238,498	G/T	—	uncertain significance
rs778326387	1:228,238,512	G/A	—	uncertain significance
rs1488574529	1:228,238,515	G/A	—	uncertain significance
rs2464481176	1:228,238,519	T/C	—	uncertain significance
rs747469469	1:228,238,520	C/T	—	likely benign
rs1003822634	1:228,238,535	G/A	—	uncertain significance
rs529067103	1:228,238,540	C/G	—	uncertain significance
rs141170201	1:228,238,550	C/T	—	likely benign
rs377685047	1:228,238,553	C/T	—	likely benign
rs61742275	1:228,238,556	C/T	—	benign
rs767429545	1:228,238,560	C/T	—	uncertain significance
rs779729203	1:228,238,570	G/A	—	uncertain significance
rs1217311405	1:228,238,594	A/G	—	uncertain significance
rs747520416	1:228,238,597	G/A	—	uncertain significance
rs145882986	1:228,238,607	C/T	—	likely benign
rs775801439	1:228,238,630	C/T	—	likely benign
rs371438338	1:228,238,631	G/A	—	likely benign
rs370461818	1:228,238,633	C/T	—	likely benign
rs371407277	1:228,238,638	G/A	—	benign
rs750280769	1:228,238,640	A/G	—	likely benign
rs774636884	1:228,246,668	T/C	—	likely benign
rs773307853	1:228,246,673	C/T	—	likely benign
rs766205520	1:228,246,676	G/T	—	likely benign
rs1279460920	1:228,246,680	C/T	—	likely benign
rs764867073	1:228,246,695	C/T	—	likely benign
rs2464499461	1:228,246,727	G/A	—	uncertain significance
rs2031739448	1:228,246,743	C/A	—	uncertain significance
rs756519375	1:228,246,762	T/C	—	uncertain significance
rs972949582	1:228,246,771	C/G	—	uncertain significance
rs776557653	1:228,246,821	C/T	—	likely benign
rs904646118	1:228,246,847	G/C	—	uncertain significance
rs2464499840	1:228,246,850	A/T	—	uncertain significance
rs775152425	1:228,246,857	C/G	—	likely benign
rs1393525016	1:228,246,869	G/T	—	uncertain significance
rs768601883	1:228,246,883	G/T	—	uncertain significance
rs2124821695	1:228,246,885	T/G	—	uncertain significance
rs1318316656	1:228,246,888	A/C	—	uncertain significance
rs761306494	1:228,246,892	A/C	—	uncertain significance
rs755419088	1:228,246,904	C/T	—	uncertain significance
rs779383747	1:228,246,905	C/G	—	likely benign
rs1352290312	1:228,246,907	C/A	—	uncertain significance

Showing 100 of 126 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.