TNIP1 c.-37+653G>C

Variant ID: 5-150459788-C-G

NM_006058.5(TNIP1):c.-37+653G>C

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Association of two independent functional risk haplotypes in TNIP1 with systemic lupus erythematosus.

Arthritis And Rheumatism
Adrianto, Indra I; Wang, Shaofeng S; Wiley, Graham B GB; Lessard, Christopher J CJ; Kelly, Jennifer A JA; Adler, Adam J AJ; Glenn, Stuart B SB; Williams, Adrienne H AH; Ziegler, Julie T JT; Comeau, Mary E ME; Marion, Miranda C MC; Wakeland, Benjamin E BE; Liang, Chaoying C; Kaufman, Kenneth M KM; Guthridge, Joel M JM; Alarcón-Riquelme, Marta E ME; , ; Alarcón, Graciela S GS; Anaya, Juan-Manuel JM; Bae, Sang-Cheol SC; Kim, Jae-Hoon JH; Joo, Young Bin YB; Boackle, Susan A SA; Brown, Elizabeth E EE; Petri, Michelle A MA; Ramsey-Goldman, Rosalind R; Reveille, John D JD; Vilá, Luis M LM; Criswell, Lindsey A LA; Edberg, Jeffrey C JC; Freedman, Barry I BI; Gilkeson, Gary S GS; Jacob, Chaim O CO; James, Judith A JA; Kamen, Diane L DL; Kimberly, Robert P RP; Martín, Javier J; Merrill, Joan T JT; Niewold, Timothy B TB; Pons-Estel, Bernardo A BA; Scofield, R Hal RH; Stevens, Anne M AM; Tsao, Betty P BP; Vyse, Timothy J TJ; Langefeld, Carl D CD; Harley, John B JB; Wakeland, Edward K EK; Moser, Kathy L KL; Montgomery, Courtney G CG; Gaffney, Patrick M PM
Publication Date: 2012-11

Variant appearance in text: rs918498
PubMed Link: 22833143
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association studies of asthma indicate opposite immunopathogenesis direction from autoimmune diseases.

The Journal Of Allergy And Clinical Immunology
Li, Xingnan X; Ampleford, Elizabeth J EJ; Howard, Timothy D TD; Moore, Wendy C WC; Torgerson, Dara G DG; Li, Huashi H; Busse, William W WW; Castro, Mario M; Erzurum, Serpil C SC; Israel, Elliot E; Nicolae, Dan L DL; Ober, Carole C; Wenzel, Sally E SE; Hawkins, Gregory A GA; Bleecker, Eugene R ER; Meyers, Deborah A DA
Publication Date: 2012-10

Variant appearance in text: rs918498
PubMed Link: 22694930
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis.

Plos Genetics
Allanore, Yannick Y; Saad, Mohamad M; Dieudé, Philippe P; Avouac, Jérôme J; Distler, Jorg H W JH; Amouyel, Philippe P; Matucci-Cerinic, Marco M; Riemekasten, Gabriella G; Airo, Paolo P; Melchers, Inga I; Hachulla, Eric E; Cusi, Daniele D; Wichmann, H-Erich HE; Wipff, Julien J; Lambert, Jean-Charles JC; Hunzelmann, Nicolas N; Tiev, Kiet K; Caramaschi, Paola P; Diot, Elisabeth E; Kowal-Bielecka, Otylia O; Valentini, Gabriele G; Mouthon, Luc L; Czirják, László L; Damjanov, Nemanja N; Salvi, Erika E; Conti, Costanza C; Müller, Martina M; Müller-Ladner, Ulf U; Riccieri, Valeria V; Ruiz, Barbara B; Cracowski, Jean-Luc JL; Letenneur, Luc L; Dupuy, Anne Marie AM; Meyer, Oliver O; Kahan, André A; Munnich, Arnold A; Boileau, Catherine C; Martinez, Maria M
Publication Date: 2011-07

Variant appearance in text: rs918498
PubMed Link: 21750679
Variant Present in the following documents:
  • pgen.1002091.pdf
View BVdb publication page