THADA

THADA armadillo repeat containing

Summary

This gene is the target of 2p21 choromosomal aberrations in benign thyroid adenomas. Single nucleotide polymorphisms (SNPs) in this gene may be associated with type 2 diabetes and polycystic ovary syndrome. The encoded protein is likely involved in the death receptor pathway and apoptosis. [provided by RefSeq, Sep 2016]

Known Variants237 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs114015985	2:43,458,097	G/A	—	uncertain significance
rs779072355	2:43,458,103	G/C	—	uncertain significance
rs755119430	2:43,458,133	G/A	—	uncertain significance
rs377552891	2:43,458,138	A/G	—	likely benign
rs748798993	2:43,458,168	T/A	—	uncertain significance
rs777910643	2:43,458,238	A/G	—	uncertain significance
rs1275076097	2:43,458,265	A/C	—	uncertain significance
rs768211032	2:43,458,281	G/A	—	uncertain significance
rs1228108356	2:43,458,301	G/C	—	uncertain significance
rs371924063	2:43,458,394	A/G	—	uncertain significance
rs756708495	2:43,458,401	G/A	—	uncertain significance
rs2103996032	2:43,458,419	C/T	—	uncertain significance
rs746648119	2:43,458,445	T/C	—	uncertain significance
rs1349315208	2:43,458,466	A/G	—	uncertain significance
rs746973767	2:43,458,467	G/A	—	likely benign
rs147386872	2:43,458,474	T/G	—	uncertain significance
rs773635027	2:43,459,878	C/T	—	uncertain significance
rs1042515153	2:43,459,890	T/A	—	uncertain significance
rs765825863	2:43,459,920	G/C	—	uncertain significance
rs199949051	2:43,459,989	C/T	—	uncertain significance
rs765660952	2:43,460,013	A/C	—	uncertain significance
rs141647229	2:43,473,222	G/C	intron variant	—
rs6745977	2:43,490,864	C/T	intron variant	—
rs763479058	2:43,506,907	T/G	—	uncertain significance
rs1026221518	2:43,506,922	T/G	—	uncertain significance
rs2466405722	2:43,506,945	A/G	—	uncertain significance
rs1421832057	2:43,506,963	T/A	—	uncertain significance
rs112504846	2:43,506,979	C/T	—	likely benign
rs377020386	2:43,514,039	G/A	—	likely benign
rs748510527	2:43,514,077	G/C	—	uncertain significance
rs1400976366	2:43,514,101	C/T	—	uncertain significance
rs372744844	2:43,514,107	C/T	—	uncertain significance
rs765010895	2:43,514,122	C/G	—	uncertain significance
rs2466456823	2:43,514,192	T/G	—	likely benign
rs17030648	2:43,518,843	A/G	—	benign
rs772904848	2:43,518,851	A/C	—	uncertain significance
rs369444028	2:43,519,264	A/G	—	uncertain significance
rs201100629	2:43,519,269	C/T	—	uncertain significance
rs34600960	2:43,519,295	G/A	—	likely benign
rs35720761	2:43,519,977	C/T	missense variant	—
rs748234890	2:43,520,047	G/C	—	uncertain significance
rs746253931	2:43,520,082	G/A	—	uncertain significance
rs765208529	2:43,520,122	G/A	—	uncertain significance
rs57257569	2:43,520,160	G/C	—	benign
rs368805649	2:43,520,181	C/T	—	likely benign
rs749703786	2:43,520,202	G/A	—	likely benign
rs1218505226	2:43,520,218	C/A	—	uncertain significance
rs2466495272	2:43,520,223	G/A	—	uncertain significance
rs1558531907	2:43,520,263	G/C	—	uncertain significance
rs10173251	2:43,529,508	C/T	—	—
rs7590268	2:43,540,125	T/G	regulatory region variant	—
rs11690012	2:43,542,480	G/C	intron variant	—
rs371006127	2:43,547,589	C/T	—	likely benign
rs1217994941	2:43,547,611	T/C	—	uncertain significance
rs752113084	2:43,547,628	T/C	—	likely benign
rs17334247	2:43,547,672	G/A	—	benign
rs73923570	2:43,551,893	A/G	intron variant	—
rs1465618	2:43,553,949	T/C	intron variant	—
rs17406174	2:43,557,484	C/G	regulatory region variant	—
rs62137415	2:43,569,728	C/T	intron variant	—
rs61754254	2:43,571,277	G/A	—	likely benign
rs1667367058	2:43,571,291	C/T	—	uncertain significance
rs1215446607	2:43,571,301	T/C	—	likely benign
rs1667372343	2:43,571,324	T/C	—	uncertain significance
rs141195177	2:43,571,333	G/A	—	likely benign
rs35422033	2:43,571,347	G/A	—	benign
rs367984894	2:43,571,360	T/C	—	uncertain significance
rs6743071	2:43,586,287	T/G	regulatory region variant	—
rs6732426	2:43,587,504	C/T	regulatory region variant	—
rs76857293	2:43,591,676	C/G	—	—
rs76215753	2:43,597,142	C/T	intron variant	—
rs10495899	2:43,602,304	G/C	intron variant	—
rs78314405	2:43,604,741	G/A	intron variant	—
rs76675804	2:43,611,883	T/C	intron variant	—
rs74616425	2:43,613,582	C/G	intron variant	—
rs11899863	2:43,618,819	C/T	regulatory region variant	—
rs10166054	2:43,619,040	T/C	regulatory region variant	—
rs79165612	2:43,624,252	A/C	intron variant	—
rs182266798	2:43,625,142	G/A	—	uncertain significance
rs771289600	2:43,625,154	C/G	—	uncertain significance
rs33979934	2:43,625,184	T/A	—	benign
rs199694887	2:43,625,188	A/G	—	likely benign
rs370231636	2:43,625,196	T/G	—	uncertain significance
rs751757187	2:43,625,214	T/C	—	uncertain significance
rs56269749	2:43,625,278	C/A	—	benign
rs57696714	2:43,626,521	T/C	intron variant	—
rs13429458	2:43,638,838	A/C	downstream gene variant	—
rs760992778	2:43,655,272	A/C	—	uncertain significance
rs1437917951	2:43,655,292	C/T	—	uncertain significance
rs374567143	2:43,655,303	C/T	—	uncertain significance
rs201128133	2:43,655,304	G/A	—	likely benign
rs2466729896	2:43,655,312	T/C	—	uncertain significance
rs935610225	2:43,655,341	C/T	—	uncertain significance
rs763522533	2:43,657,398	G/A	—	uncertain significance
rs749886006	2:43,657,415	C/T	—	uncertain significance
rs2466741069	2:43,657,419	A/G	—	uncertain significance
rs568331233	2:43,659,180	A/G	—	—
rs75126888	2:43,664,007	C/T	intron variant	—
rs76684055	2:43,665,943	G/A	regulatory region variant	—
rs111812200	2:43,674,278	T/C	intron variant	—

Showing 100 of 237 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.