EXD3

exonuclease 3'-5' domain containing 3

Summary

Predicted to enable 3'-5' exonuclease activity; metal ion binding activity; and nucleic acid binding activity. Predicted to be involved in nucleobase-containing compound metabolic process. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants104 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs200221658	9:140,201,415	C/G	—	uncertain significance
rs766166062	9:140,201,430	G/A	—	uncertain significance
rs752477082	9:140,201,443	C/T	—	uncertain significance
rs771710735	9:140,201,475	C/T	—	uncertain significance
rs375831870	9:140,201,493	C/T	—	uncertain significance
rs200899844	9:140,201,494	G/A	—	uncertain significance
rs775413905	9:140,201,509	C/T	—	uncertain significance
rs748448428	9:140,201,541	C/T	—	uncertain significance
rs377386003	9:140,201,605	G/A	—	uncertain significance
rs199943268	9:140,201,614	C/T	—	likely benign
rs780776396	9:140,201,619	A/G	—	uncertain significance
rs915690761	9:140,202,074	G/C	—	uncertain significance
rs368951605	9:140,202,093	C/T	—	likely benign
rs749540431	9:140,204,064	C/T	—	uncertain significance
rs1158927150	9:140,204,116	C/A	—	uncertain significance
rs199671547	9:140,204,125	C/A	—	uncertain significance
rs573550533	9:140,204,127	T/C	—	uncertain significance
rs150312520	9:140,218,184	C/T	—	uncertain significance
rs2538945574	9:140,218,206	T/C	—	uncertain significance
rs200104609	9:140,218,283	C/T	—	uncertain significance
rs771592009	9:140,218,304	C/G	—	uncertain significance
rs368208485	9:140,218,305	G/A	—	uncertain significance
rs775469023	9:140,218,564	G/A	—	uncertain significance
rs949943356	9:140,229,338	G/C	—	—
rs765802505	9:140,242,530	G/A	—	uncertain significance
rs367737146	9:140,242,576	C/G	—	uncertain significance
rs376214483	9:140,242,593	C/A	—	uncertain significance
rs764339032	9:140,242,594	G/A	—	uncertain significance
rs770651255	9:140,243,611	C/T	—	likely benign
rs563416988	9:140,243,612	G/A	—	uncertain significance
rs1361164548	9:140,243,623	C/G	—	uncertain significance
rs2538995902	9:140,243,668	A/C	—	uncertain significance
rs200918724	9:140,243,678	G/A	—	likely benign
rs180673666	9:140,243,726	C/T	—	uncertain significance
rs1430392416	9:140,243,833	C/T	—	uncertain significance
rs1289208703	9:140,243,856	C/T	—	uncertain significance
rs370151337	9:140,243,857	G/A	—	uncertain significance
rs200106940	9:140,243,868	G/A	—	uncertain significance
rs35097575	9:140,243,880	G/A	—	benign
rs372535992	9:140,243,953	C/T	—	uncertain significance
rs571541545	9:140,243,979	C/T	—	uncertain significance
rs2539000910	9:140,245,545	G/C	—	uncertain significance
rs575148945	9:140,245,599	C/G	—	uncertain significance
rs760243505	9:140,245,793	G/A	—	uncertain significance
rs377284984	9:140,245,800	G/A	—	uncertain significance
rs201793473	9:140,245,916	C/T	—	uncertain significance
rs548894905	9:140,245,917	G/A	—	uncertain significance
rs548116967	9:140,245,922	C/T	—	uncertain significance
rs773753469	9:140,245,925	C/T	—	uncertain significance
rs370098734	9:140,246,586	G/T	—	uncertain significance
rs763146329	9:140,246,643	C/A	—	uncertain significance
rs369396971	9:140,247,085	T/C	—	uncertain significance
rs1251691554	9:140,247,118	G/A	—	uncertain significance
rs1006461205	9:140,247,130	C/T	—	uncertain significance
rs370293169	9:140,247,165	G/A	—	uncertain significance
rs1161549206	9:140,247,221	G/T	—	uncertain significance
rs73581564	9:140,247,497	A/C	intron variant	—
rs753572717	9:140,248,824	G/C	—	uncertain significance
rs911492390	9:140,249,163	G/A	—	uncertain significance
rs746627625	9:140,249,166	T/C	—	uncertain significance
rs201798904	9:140,249,195	C/T	—	uncertain significance
rs187592184	9:140,249,196	G/A	—	uncertain significance
rs751957112	9:140,249,225	G/A	—	uncertain significance
rs570353658	9:140,250,722	G/A	—	uncertain significance
rs201678237	9:140,250,729	C/T	—	uncertain significance
rs200783001	9:140,250,737	C/T	—	uncertain significance
rs368890121	9:140,250,776	G/A	—	uncertain significance
rs749508701	9:140,250,786	T/C	—	uncertain significance
rs76472430	9:140,250,808	C/T	—	likely benign
rs371300749	9:140,250,816	A/G	—	uncertain significance
rs761128296	9:140,250,819	G/A	—	uncertain significance
rs113727800	9:140,258,802	G/A	intron variant	—
rs367988278	9:140,261,027	C/T	—	uncertain significance
rs1288769405	9:140,261,054	C/A	—	uncertain significance
rs756751194	9:140,262,396	C/T	—	uncertain significance
rs953984580	9:140,262,399	C/A	—	uncertain significance
rs372549468	9:140,262,407	G/A	—	uncertain significance
rs11507683	9:140,262,424	C/G	synonymous variant	—
rs765116513	9:140,262,425	G/A	—	uncertain significance
rs769774272	9:140,267,385	C/T	—	uncertain significance
rs771121580	9:140,267,403	A/G	—	uncertain significance
rs534339635	9:140,267,432	G/C	—	uncertain significance
rs368323331	9:140,267,454	G/A	—	likely benign
rs371916480	9:140,267,467	G/A	—	uncertain significance
rs751921821	9:140,267,468	G/T	—	uncertain significance
rs761397122	9:140,267,469	C/A	—	uncertain significance
rs1460315393	9:140,267,502	A/C	—	uncertain significance
rs201919795	9:140,267,503	G/C	—	uncertain significance
rs373202434	9:140,267,907	G/C	—	uncertain significance
rs200745627	9:140,267,930	G/T	—	uncertain significance
rs528218403	9:140,267,973	G/A	—	uncertain significance
rs200337667	9:140,267,982	C/T	—	uncertain significance
rs752788688	9:140,267,991	C/T	—	uncertain significance
rs762400259	9:140,268,012	C/T	—	uncertain significance
rs767296342	9:140,268,029	C/T	—	uncertain significance
rs763297297	9:140,277,772	C/T	—	uncertain significance
rs1342545888	9:140,277,773	G/A	—	uncertain significance
rs764009655	9:140,277,778	C/T	—	uncertain significance
rs999103043	9:140,277,781	G/A	—	uncertain significance
rs778228218	9:140,277,818	G/C	—	uncertain significance

Showing 100 of 104 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.