AHDC1

AT-hook DNA binding motif containing 1

Summary

This gene encodes a protein containing two AT-hooks, which likely function in DNA binding. Mutations in this gene were found in individuals with Xia-Gibbs syndrome. [provided by RefSeq, Jun 2014]

Known Variants925 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs149147457	1:27,873,830	G/A	—	likely benign
rs2019213941	1:27,873,837	G/C	—	uncertain significance
rs61742782	1:27,873,845	G/A	—	likely benign
rs778493358	1:27,873,858	G/A	—	likely benign
rs1421962085	1:27,873,862	T/C	—	uncertain significance
rs895223934	1:27,873,866	C/A	—	likely benign
rs771516746	1:27,873,875	G/A	—	likely benign
rs774871172	1:27,873,877	C/T	—	uncertain significance
rs747550510	1:27,873,878	G/A	—	likely benign
rs2521768678	1:27,873,888	C/A	—	uncertain significance
rs141730488	1:27,873,895	C/T	—	uncertain significance
rs371087154	1:27,873,909	G/A	—	conflicting classifications of pathogenicity
rs2148254934	1:27,873,910	C/A	—	likely benign
rs539447084	1:27,873,940	C/T	—	conflicting classifications of pathogenicity
rs750016023	1:27,873,941	G/A	—	likely benign
rs1571224398	1:27,873,948	T/A	—	uncertain significance
rs2019226046	1:27,873,953	G/A	—	likely benign
rs368785856	1:27,873,960	A/T	—	uncertain significance
rs781513175	1:27,873,963	G/A	—	likely benign
rs372231427	1:27,873,972	G/A	—	likely benign
rs375725827	1:27,873,976	C/A	—	uncertain significance
rs753712788	1:27,873,977	G/A	—	likely benign
rs369828844	1:27,873,981	G/T	—	uncertain significance
rs779614929	1:27,873,985	G/A	—	likely benign
rs1164997538	1:27,874,006	G/A	—	uncertain significance
rs193153262	1:27,874,024	C/T	—	likely benign
rs930508757	1:27,874,032	G/A	—	uncertain significance
rs754657004	1:27,874,041	C/T	—	uncertain significance
rs200178921	1:27,874,042	G/A	—	likely benign
rs761729007	1:27,874,044	G/A	—	conflicting classifications of pathogenicity
rs943215779	1:27,874,054	G/C	—	likely benign
rs2521783316	1:27,874,056	G/T	—	uncertain significance
rs2019235069	1:27,874,058	C/T	—	likely benign
rs370031268	1:27,874,059	C/T	—	likely benign
rs766220211	1:27,874,060	G/A	—	conflicting classifications of pathogenicity
rs1363372692	1:27,874,065	A/G	—	uncertain significance
rs2019236041	1:27,874,066	T/C	—	uncertain significance
rs2019237372	1:27,874,081	T/C	—	uncertain significance
rs752303184	1:27,874,084	C/T	—	conflicting classifications of pathogenicity
rs139569820	1:27,874,094	C/T	—	benign
rs998488441	1:27,874,104	G/A	—	likely benign
rs1031272518	1:27,874,107	C/T	—	benign
rs757909215	1:27,874,115	G/A	—	likely benign
rs2019240667	1:27,874,119	G/A	—	uncertain significance
rs2019240985	1:27,874,122	G/A	—	uncertain significance
rs2521789659	1:27,874,125	C/A	—	uncertain significance
rs747135569	1:27,874,130	G/A	—	likely benign
rs368578678	1:27,874,133	C/T	—	likely benign
rs762961815	1:27,874,134	G/A	—	uncertain significance
rs201460329	1:27,874,135	C/T	—	likely benign
rs781635710	1:27,874,136	G/A	—	likely benign
rs752427666	1:27,874,143	G/A	—	likely benign
rs1414986918	1:27,874,148	G/A	—	uncertain significance
rs1571225433	1:27,874,153	G/A	—	likely benign
rs373346553	1:27,874,154	G/A	—	likely benign
rs563340018	1:27,874,178	C/T	—	uncertain significance
rs2019246687	1:27,874,195	G/A	—	uncertain significance
rs758589491	1:27,874,196	C/T	—	likely benign
rs1037389786	1:27,874,197	G/A	—	likely benign
rs374027631	1:27,874,198	G/A	—	likely benign
rs746396362	1:27,874,203	C/T	—	uncertain significance
rs747256157	1:27,874,204	G/A	—	likely benign
rs2019248403	1:27,874,209	G/A	—	uncertain significance
rs1321892195	1:27,874,223	G/T	—	likely pathogenic
rs1291837711	1:27,874,235	T/A	—	likely benign
rs145080672	1:27,874,243	T/G	—	likely benign
rs1207697746	1:27,874,250	G/A	—	likely benign
rs2019251885	1:27,874,251	G/C	—	uncertain significance
rs1222986671	1:27,874,253	G/A	—	likely benign
rs1557655967	1:27,874,257	T/C	—	likely benign
rs775223166	1:27,874,258	C/T	—	uncertain significance
rs200725386	1:27,874,259	G/A	—	benign
rs753448843	1:27,874,264	G/A	—	uncertain significance
rs2521800916	1:27,874,270	G/T	—	uncertain significance
rs1161659394	1:27,874,271	G/A	—	likely benign
rs1316459609	1:27,874,277	C/T	—	likely benign
rs377174668	1:27,874,278	G/A	—	conflicting classifications of pathogenicity
rs1337874441	1:27,874,288	G/A	—	conflicting classifications of pathogenicity
rs751713431	1:27,874,292	G/T	—	likely benign
rs199527867	1:27,874,298	G/C	—	likely benign
rs1196298684	1:27,874,303	C/T	—	uncertain significance
rs1425646468	1:27,874,309	C/T	—	uncertain significance
rs769793074	1:27,874,311	G/A	—	uncertain significance
rs566131872	1:27,874,319	G/A	—	likely benign
rs1461582216	1:27,874,332	G/T	—	uncertain significance
rs368747937	1:27,874,334	C/G	—	likely benign
rs1553158013	1:27,874,336	C/T	—	uncertain significance
rs1394609801	1:27,874,338	T/C	—	uncertain significance
rs1571226426	1:27,874,346	A/G	—	likely benign
rs372813656	1:27,874,347	T/C	—	conflicting classifications of pathogenicity
rs1298824243	1:27,874,354	G/A	—	uncertain significance
rs527518359	1:27,874,358	C/G	—	uncertain significance
rs775977549	1:27,874,360	C/T	—	likely benign
rs375964883	1:27,874,361	G/A	—	likely benign
rs142913680	1:27,874,364	G/C	—	likely benign
rs2521809613	1:27,874,368	G/C	—	uncertain significance
rs1426674008	1:27,874,370	C/T	—	likely benign
rs547570973	1:27,874,373	C/T	—	likely benign
rs1427943290	1:27,874,376	T/A	—	likely benign
rs141082682	1:27,874,383	G/A	—	likely benign

Showing 100 of 925 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.