NID1

nidogen 1

Summary

This gene encodes a member of the nidogen family of basement membrane glycoproteins. The protein interacts with several other components of basement membranes, and may play a role in cell interactions with the extracellular matrix. [provided by RefSeq, Jul 2008]

Known Variants171 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs3213190	1:236,141,174	T/C	—	benign
rs6662744	1:236,141,234	G/A	—	likely benign
rs1572572600	1:236,141,253	T/C	—	uncertain significance
rs144862964	1:236,141,259	C/T	—	uncertain significance
rs145374651	1:236,141,273	G/A	—	uncertain significance
rs12032474	1:236,142,253	T/G	—	benign
rs770056148	1:236,142,331	A/T	—	uncertain significance
rs11580785	1:236,142,411	C/T	—	benign
rs1536132	1:236,142,565	C/T	—	benign
rs3738524	1:236,142,570	C/G	—	benign
rs16833032	1:236,143,144	G/C	—	benign
rs780410514	1:236,143,207	T/A	—	uncertain significance
rs944090942	1:236,143,236	C/A	—	uncertain significance
rs730882225	1:236,143,795	C/T	—	pathogenic
rs753202272	1:236,143,861	T/A	—	uncertain significance
rs267598426	1:236,143,879	C/T	—	uncertain significance
rs769647164	1:236,143,887	C/T	—	likely benign
rs201035097	1:236,143,898	T/C	—	uncertain significance
rs3820557	1:236,144,261	T/C	—	benign
rs3820558	1:236,144,754	C/A	—	benign
rs145820513	1:236,144,919	G/T	—	benign
rs3738525	1:236,144,951	A/G	—	benign
rs371251887	1:236,145,007	C/T	—	uncertain significance
rs2527862721	1:236,145,022	T/C	—	uncertain significance
rs142891889	1:236,145,040	C/T	—	uncertain significance
rs715956	1:236,145,145	T/C	—	benign
rs715957	1:236,145,289	A/G	—	benign
rs2527868483	1:236,148,747	T/C	—	uncertain significance
rs140746746	1:236,148,787	G/T	—	uncertain significance
rs2182119	1:236,149,054	G/A	—	benign
rs1041111	1:236,154,012	T/C	—	benign
rs150114110	1:236,154,187	G/A	—	uncertain significance
rs753910999	1:236,154,193	T/C	—	uncertain significance
rs16833060	1:236,154,206	T/C	—	benign
rs780745362	1:236,154,292	G/A	—	uncertain significance
rs147031904	1:236,154,308	C/T	—	uncertain significance
rs138322087	1:236,154,319	G/A	—	likely benign
rs1297851350	1:236,154,337	G/A	—	uncertain significance
rs4660137	1:236,154,365	G/T	—	benign
rs1014635275	1:236,156,954	T/G	—	uncertain significance
rs201356535	1:236,157,033	G/A	—	benign
rs149027520	1:236,157,059	G/A	—	uncertain significance
rs917113229	1:236,157,121	G/C	—	uncertain significance
rs17854360	1:236,157,123	T/C	—	benign
rs1657838274	1:236,157,137	G/C	—	uncertain significance
rs2527883016	1:236,157,138	T/G	—	uncertain significance
rs147665041	1:236,157,150	C/G	—	uncertain significance
rs16833075	1:236,157,277	T/G	—	benign
rs10495369	1:236,157,433	A/T	—	benign
rs2031486	1:236,175,153	T/C	—	benign
rs771612950	1:236,175,230	C/T	—	uncertain significance
rs760250427	1:236,175,235	C/T	—	likely benign
rs776307572	1:236,175,242	C/T	—	uncertain significance
rs3738530	1:236,175,309	A/T	—	benign
rs979143011	1:236,175,320	G/C	—	uncertain significance
rs3738531	1:236,175,327	C/A	—	benign
rs2031487	1:236,175,339	T/C	—	benign
rs200447099	1:236,175,351	A/G	—	benign
rs6669467	1:236,175,585	C/T	—	benign
rs148665567	1:236,176,777	T/G	—	likely benign
rs779358669	1:236,176,794	C/T	—	uncertain significance
rs372753135	1:236,176,833	T/C	—	uncertain significance
rs10803217	1:236,176,990	C/T	—	benign
rs3754237	1:236,177,182	A/G	—	benign
rs3768080	1:236,179,869	A/G	intron variant	—
rs11577753	1:236,180,180	A/C	—	benign
rs758330404	1:236,180,475	G/C	—	uncertain significance
rs375679312	1:236,180,493	C/T	—	uncertain significance
rs140374909	1:236,180,498	C/T	—	benign
rs141204959	1:236,180,504	G/T	—	conflicting classifications of pathogenicity
rs376020558	1:236,180,514	G/A	—	uncertain significance
rs373911691	1:236,180,568	C/T	—	uncertain significance
rs3768081	1:236,180,580	C/G	—	benign
rs10754833	1:236,184,931	T/G	—	—
rs3738533	1:236,187,365	T/C	—	benign
rs138933538	1:236,187,372	T/C	—	likely benign
rs149309893	1:236,187,393	C/T	—	uncertain significance
rs143743775	1:236,187,413	G/A	—	benign
rs146611286	1:236,187,450	G/A	—	uncertain significance
rs3738534	1:236,187,492	T/C	—	benign
rs199655594	1:236,189,209	A/C	—	uncertain significance
rs576525237	1:236,189,210	A/G	—	uncertain significance
rs1373359316	1:236,189,253	T/G	—	uncertain significance
rs143707993	1:236,189,269	G/T	—	uncertain significance
rs16833131	1:236,189,278	C/T	—	benign
rs779454402	1:236,189,300	A/T	—	uncertain significance
rs1296913608	1:236,189,318	T/C	—	uncertain significance
rs906473040	1:236,189,393	C/T	—	likely benign
rs535886435	1:236,189,397	C/T	—	uncertain significance
rs1420460554	1:236,189,410	C/T	—	likely benign
rs10803233	1:236,189,722	G/T	—	benign
rs6429477	1:236,192,555	C/G	—	benign
rs6693929	1:236,192,673	C/G	—	benign
rs3818238	1:236,192,782	G/A	—	benign
rs769851347	1:236,192,855	G/A	—	uncertain significance
rs1283643455	1:236,192,891	T/G	—	uncertain significance
rs536352898	1:236,192,904	C/T	—	uncertain significance
rs774575082	1:236,192,909	G/A	—	uncertain significance
rs370617487	1:236,192,917	C/T	—	likely benign
rs751460426	1:236,192,925	G/A	—	uncertain significance

Showing 100 of 171 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.