MMP3 c.935+368G>A

Variant ID: 11-102710471-C-T

NM_002422.3(MMP3):c.935+368G>A

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Genome-wide association study of peripheral artery disease in the Million Veteran Program.

Nature Medicine
Klarin, Derek D; Lynch, Julie J; Aragam, Krishna K; Chaffin, Mark M; Assimes, Themistocles L TL; Huang, Jie J; Lee, Kyung Min KM; Shao, Qing Q; Huffman, Jennifer E JE; Natarajan, Pradeep P; Arya, Shipra S; Small, Aeron A; Sun, Yan V YV; Vujkovic, Marijana M; Freiberg, Matthew S MS; Wang, Lu L; Chen, Jinbo J; Saleheen, Danish D; Lee, Jennifer S JS; Miller, Donald R DR; Reaven, Peter P; Alba, Patrick R PR; Patterson, Olga V OV; DuVall, Scott L SL; Boden, William E WE; Beckman, Joshua A JA; Gaziano, J Michael JM; Concato, John J; Rader, Daniel J DJ; Cho, Kelly K; Chang, Kyong-Mi KM; Wilson, Peter W F PWF; O'Donnell, Christopher J CJ; Kathiresan, Sekar S; , ; Tsao, Philip S PS; Damrauer, Scott M SM
Publication Date: 2019-08

Variant appearance in text: rs566125
PubMed Link: 31285632
Variant Present in the following documents:
  • Main text
  • nihms-1529756.pdf
View BVdb publication page



Associations between SNPs and immune-related circulating proteins in schizophrenia.

Scientific Reports
Chan, Man K MK; Cooper, Jason D JD; Heilmann-Heimbach, Stefanie S; Frank, Josef J; Witt, Stephanie H SH; Nöthen, Markus M MM; Steiner, Johann J; Rietschel, Marcella M; Bahn, Sabine S
Publication Date: 2017-10-03

Variant appearance in text: rs566125
PubMed Link: 28974776
Variant Present in the following documents:
  • Main text
  • 41598_2017_Article_12986.pdf
View BVdb publication page



Genetic adaptation of the human circadian clock to day-length latitudinal variations and relevance for affective disorders.

Genome Biology
Forni, Diego D; Pozzoli, Uberto U; Cagliani, Rachele R; Tresoldi, Claudia C; Menozzi, Giorgia G; Riva, Stefania S; Guerini, Franca R FR; Comi, Giacomo P GP; Bolognesi, Elisabetta E; Bresolin, Nereo N; Clerici, Mario M; Sironi, Manuela M
Publication Date: 2014

Variant appearance in text: rs566125
PubMed Link: 25358694
Variant Present in the following documents:
  • Main text
  • 13059_2014_Article_499.pdf
View BVdb publication page



Matrix metalloproteinases 2 and 3 gene polymorphisms and the risk of target vessel revascularization after percutaneous coronary intervention: Is there still room for determining genetic variation of MMPs for assessment of an increased risk of restenosis?

Disease Markers
Verschuren, J J W JJ; Sampietro, M L ML; Pons, D D; Trompet, S S; Ewing, M M MM; Quax, P H A PH; de Knijff, P P; Zwinderman, A H AH; de Winter, R J RJ; Tio, R A RA; de Maat, M P MP; Doevendans, P A F M PA; Jukema, J W JW
Publication Date: 2010

Variant appearance in text: rs566125
PubMed Link: 21206012
Variant Present in the following documents:
  • DM29-05-504039.pdf
View BVdb publication page



Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes.

Bmc Medical Genetics
Larson, Martin G MG; Atwood, Larry D LD; Benjamin, Emelia J EJ; Cupples, L Adrienne LA; D'Agostino, Ralph B RB; Fox, Caroline S CS; Govindaraju, Diddahally R DR; Guo, Chao-Yu CY; Heard-Costa, Nancy L NL; Hwang, Shih-Jen SJ; Murabito, Joanne M JM; Newton-Cheh, Christopher C; O'Donnell, Christopher J CJ; Seshadri, Sudha S; Vasan, Ramachandran S RS; Wang, Thomas J TJ; Wolf, Philip A PA; Levy, Daniel D
Publication Date: 2007-09-19

Variant appearance in text: rs566125
PubMed Link: 17903304
Variant Present in the following documents:
  • Main text
  • 1471-2350-8-S1-S5.pdf
View BVdb publication page