NID2

nidogen 2

Summary

This gene encodes a member of the nidogen family of basement membrane proteins. This protein is a cell-adhesion protein that binds collagens I and IV and laminin and may be involved in maintaining the structure of the basement membrane.[provided by RefSeq, Jun 2010]

Known Variants129 total

rsidPosition (GRCh37)AllelesClassClinVar
rs74841261614:52,472,464A/G—uncertain significance
rs14902106514:52,472,502C/G—uncertain significance
rs18196622914:52,472,521C/G—uncertain significance
rs13959950114:52,473,280G/A—likely benign
rs102087620514:52,474,630A/C—uncertain significance
rs250300890014:52,474,667G/C—uncertain significance
rs13881182814:52,477,635A/G—likely benign
rs189098979614:52,477,653C/G—uncertain significance
rs250301953114:52,477,670C/A—uncertain significance
rs37070306214:52,477,679C/T—uncertain significance
rs20064115914:52,477,708G/A—uncertain significance
rs37013551214:52,477,727G/A—uncertain significance
rs250301996414:52,477,729A/G—uncertain significance
rs144612068314:52,477,738A/G—uncertain significance
rs36827226414:52,478,286G/A—uncertain significance
rs75555800414:52,478,307T/G—uncertain significance
rs77886854814:52,478,314C/T—likely benign
rs189102848514:52,478,317C/T—uncertain significance
rs95541727614:52,478,319C/T—uncertain significance
rs55445193214:52,478,367C/T—uncertain significance
rs77937268014:52,478,382A/G—uncertain significance
rs76043503614:52,481,045C/G—uncertain significance
rs14883427514:52,481,132C/T—uncertain significance
rs74689518514:52,481,144C/T—uncertain significance
rs129401691114:52,481,799G/A—uncertain significance
rs11296937314:52,481,810A/G—uncertain significance
rs37189368914:52,481,843A/C—uncertain significance
rs14212518514:52,481,847C/T—uncertain significance
rs6174762414:52,481,899G/T—benign
rs89614443714:52,481,901G/A—uncertain significance
rs146174181514:52,481,904C/T—uncertain significance
rs55345743614:52,481,916C/T—uncertain significance
rs74909251414:52,481,918C/G—uncertain significance
rs250304537214:52,485,796T/G—uncertain significance
rs250304577114:52,485,848C/T—likely benign
rs77622785014:52,485,852G/T—uncertain significance
rs250304612114:52,485,910T/C—uncertain significance
rs141987477914:52,485,912C/A—uncertain significance
rs13902173214:52,485,938G/A—uncertain significance
rs250304650814:52,485,961G/A—uncertain significance
rs77407546714:52,485,973C/T—uncertain significance
rs76351358414:52,485,994G/T—likely benign
rs78062682414:52,485,995T/C—uncertain significance
rs14477405914:52,486,783T/C—likely benign
rs14856880914:52,486,810C/T—uncertain significance
rs77185576614:52,486,813G/T—uncertain significance
rs143786027014:52,486,819A/G—uncertain significance
rs800716614:52,486,850G/A—benign
rs149707614:52,491,675T/A——
rs6197155514:52,492,303G/Aregulatory region variant—
rs6197155714:52,493,984T/C—uncertain significance
rs2850758714:52,493,996C/T—benign
rs134042453714:52,494,008G/C—uncertain significance
rs5587443714:52,494,637C/Aintron variant—
rs75660141114:52,495,482G/A—uncertain significance
rs14222843614:52,495,539G/T—uncertain significance
rs77512537214:52,495,540A/C—uncertain significance
rs14961470314:52,496,301C/T—uncertain significance
rs14391225214:52,496,336T/C—uncertain significance
rs100589275414:52,496,345G/A—uncertain significance
rs14834709014:52,496,373C/T—likely benign
rs6197155914:52,496,390G/A—benign
rs15090860214:52,496,399C/T—likely benign
rs19955564714:52,496,406C/T—uncertain significance
rs37409755914:52,505,540G/A—uncertain significance
rs3514793014:52,505,546C/T—likely benign
rs77591759414:52,505,566G/A—uncertain significance
rs11154055314:52,505,575G/A—uncertain significance
rs77114017314:52,505,610G/C—uncertain significance
rs14816869914:52,505,627G/A—uncertain significance
rs250310638014:52,505,668T/C—uncertain significance
rs74994642714:52,505,669A/C—uncertain significance
rs20013782714:52,505,684T/C—uncertain significance
rs53711535214:52,505,689G/T—uncertain significance
rs11375972914:52,507,359T/G—benign
rs11678045414:52,507,512C/T—benign
rs14260189514:52,507,513G/C—uncertain significance
rs20021515814:52,507,564C/G—uncertain significance
rs6174758514:52,508,842C/A—benign
rs104202689314:52,508,894G/A—uncertain significance
rs14539126514:52,508,982C/T—uncertain significance
rs74831638714:52,509,043T/G—uncertain significance
rs147187999414:52,509,560C/T—uncertain significance
rs11198903614:52,509,601C/T—likely benign
rs115715726314:52,509,606G/T—uncertain significance
rs11583379414:52,509,631G/C—conflicting classifications of pathogenicity
rs250311981114:52,509,644T/C—uncertain significance
rs7576642514:52,511,911G/Cregulatory region variant—
rs7982389014:52,511,969G/Tregulatory region variant—
rs156612914:52,514,912T/Cintron variant—
rs274988214:52,515,259T/Gintron variant—
rs73053214:52,518,811G/Aregulatory region variant—
rs13794186214:52,520,302G/A—benign
rs74583644714:52,520,350C/T—uncertain significance
rs116902305014:52,520,366G/C—uncertain significance
rs75644175014:52,520,395A/G—uncertain significance
rs36995154014:52,520,422A/T—uncertain significance
rs15103283314:52,520,480C/T—uncertain significance
rs76501037414:52,520,524C/G—uncertain significance
rs134534472814:52,520,537G/C—uncertain significance

Showing 100 of 129 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.