ZDBF2

zinc finger DBF-type containing 2

Summary

This gene encodes a protein containing DBF4-type zinc finger domains. This gene is imprinted and paternally expressed in lymphocytes but is more stochastically expressed in the placenta. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2015]

Known Variants224 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs527983736	2:207,137,604	T/C	—	—
rs142275419	2:207,143,061	A/G	intron variant	—
rs368137799	2:207,146,640	G/A	—	benign
rs2470480625	2:207,161,981	T/C	—	likely benign
rs1190672560	2:207,162,006	C/G	—	uncertain significance
rs978723909	2:207,162,024	T/C	—	uncertain significance
rs776543980	2:207,162,025	G/T	—	uncertain significance
rs2470481295	2:207,162,027	A/G	—	uncertain significance
rs116382753	2:207,162,033	G/A	—	benign
rs1476227939	2:207,162,093	A/G	—	uncertain significance
rs144743110	2:207,169,424	C/T	—	benign
rs114752443	2:207,169,486	A/G	—	benign
rs149317779	2:207,169,548	A/T	—	benign
rs943489861	2:207,169,557	C/G	—	uncertain significance
rs779996852	2:207,169,562	G/A	—	uncertain significance
rs199768532	2:207,169,576	C/T	—	likely benign
rs754236342	2:207,169,599	A/T	—	uncertain significance
rs755604527	2:207,169,602	T/G	—	uncertain significance
rs371478964	2:207,169,635	C/T	—	uncertain significance
rs143619911	2:207,169,636	G/A	—	likely benign
rs113954798	2:207,169,638	A/G	—	likely benign
rs372426207	2:207,169,649	G/A	—	likely benign
rs2470531573	2:207,169,674	T/A	—	uncertain significance
rs568368740	2:207,169,694	C/G	—	uncertain significance
rs1472869447	2:207,169,705	T/A	—	uncertain significance
rs2470532385	2:207,169,724	A/C	—	uncertain significance
rs10932150	2:207,169,731	G/A	—	benign
rs200984813	2:207,169,736	T/G	—	uncertain significance
rs2470534370	2:207,169,836	C/T	—	uncertain significance
rs745977464	2:207,169,871	T/G	—	uncertain significance
rs200044367	2:207,169,918	C/A	—	benign
rs188123543	2:207,170,002	G/A	—	benign
rs59158496	2:207,170,004	A/G	—	benign
rs77622365	2:207,170,026	T/C	—	benign
rs115212375	2:207,170,040	G/A	—	benign
rs750742601	2:207,170,087	G/T	—	uncertain significance
rs756377343	2:207,170,097	T/C	—	uncertain significance
rs373815481	2:207,170,122	A/G	—	likely benign
rs377262471	2:207,170,182	G/A	—	likely benign
rs58488107	2:207,170,197	G/T	—	benign
rs112075178	2:207,170,242	T/C	—	benign
rs2470540194	2:207,170,292	T/G	—	uncertain significance
rs759643266	2:207,170,306	G/T	—	uncertain significance
rs202036087	2:207,170,334	G/C	—	conflicting classifications of pathogenicity
rs58649882	2:207,170,344	G/T	—	benign
rs201372498	2:207,170,388	A/G	—	uncertain significance
rs759326102	2:207,170,418	A/G	—	uncertain significance
rs370689526	2:207,170,445	A/T	—	uncertain significance
rs190625973	2:207,170,456	A/G	—	uncertain significance
rs750779147	2:207,170,484	G/T	—	uncertain significance
rs1360990431	2:207,170,487	C/G	—	uncertain significance
rs141439557	2:207,170,490	C/G	—	uncertain significance
rs1375137397	2:207,170,528	A/G	—	uncertain significance
rs1359776325	2:207,170,547	A/G	—	uncertain significance
rs147458165	2:207,170,555	C/T	—	likely benign
rs769572660	2:207,170,556	G/A	—	conflicting classifications of pathogenicity
rs200447534	2:207,170,615	G/T	—	likely benign
rs758097627	2:207,170,620	C/T	—	likely benign
rs377156770	2:207,170,712	A/G	—	uncertain significance
rs763841319	2:207,170,727	C/T	—	uncertain significance
rs139933444	2:207,170,734	G/A	—	benign
rs2470547783	2:207,170,744	T/C	—	uncertain significance
rs113062013	2:207,171,030	T/C	—	uncertain significance
rs749668953	2:207,171,042	A/C	—	uncertain significance
rs192447754	2:207,171,050	G/A	—	uncertain significance
rs201581344	2:207,171,088	A/G	—	likely benign
rs78386861	2:207,171,102	G/A	—	benign
rs2470554548	2:207,171,126	A/G	—	likely benign
rs201441967	2:207,171,261	T/C	—	uncertain significance
rs192597586	2:207,171,311	C/T	—	benign
rs116303450	2:207,171,312	G/A	—	benign
rs184921981	2:207,171,359	C/T	—	uncertain significance
rs188595104	2:207,171,384	C/T	—	uncertain significance
rs1477153547	2:207,171,399	A/G	—	uncertain significance
rs368129483	2:207,171,410	G/C	—	likely benign
rs2470558391	2:207,171,412	T/A	—	uncertain significance
rs776850952	2:207,171,464	A/G	—	uncertain significance
rs751900875	2:207,171,551	C/T	—	likely benign
rs544074324	2:207,171,572	C/T	—	uncertain significance
rs2470560922	2:207,171,586	G/C	—	likely benign
rs1002958346	2:207,171,628	T/A	—	uncertain significance
rs561719362	2:207,171,726	G/A	—	uncertain significance
rs149849516	2:207,171,789	T/G	—	uncertain significance
rs780940987	2:207,171,820	G/A	—	likely benign
rs762352411	2:207,171,857	G/C	—	uncertain significance
rs148587086	2:207,171,873	C/T	—	likely benign
rs200182053	2:207,171,885	C/G	—	uncertain significance
rs762656637	2:207,172,040	C/T	—	uncertain significance
rs142490458	2:207,172,046	G/A	—	likely benign
rs2470567315	2:207,172,061	G/A	—	likely benign
rs768387234	2:207,172,136	G/A	—	likely benign
rs201022296	2:207,172,142	C/T	—	likely benign
rs1317586341	2:207,172,143	T/C	—	uncertain significance
rs377449307	2:207,172,152	C/T	—	likely benign
rs1355919398	2:207,172,164	C/T	—	uncertain significance
rs777989080	2:207,172,197	G/A	—	likely benign
rs370841894	2:207,172,207	C/T	—	benign
rs541807210	2:207,172,208	G/A	—	conflicting classifications of pathogenicity
rs764939702	2:207,172,275	A/G	—	uncertain significance
rs753023648	2:207,172,278	A/G	—	uncertain significance

Showing 100 of 224 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.