ADAMTS7 c.622+556A>G

Variant ID: 15-79089734-T-C

NM_014272.3(ADAMTS7):c.622+556A>G

This variant was identified in 6 publications

View GRCh38 version.




Publications:


ADAMTS proteins in human disorders.

Matrix Biology : Journal Of The International Society For Matrix Biology
Mead, Timothy J TJ; Apte, Suneel S SS
Publication Date: 2018-10

Variant appearance in text: rs7177699
PubMed Link: 29885460
Variant Present in the following documents:
  • Main text
View BVdb publication page



Modeling the Causal Role of DNA Methylation in the Association Between Cigarette Smoking and Inflammation in African Americans: A 2-Step Epigenetic Mendelian Randomization Study.

American Journal Of Epidemiology
Jhun, Min A MA; Smith, Jennifer A JA; Ware, Erin B EB; Kardia, Sharon L R SLR; Mosley, Thomas H TH; Turner, Stephen T ST; Peyser, Patricia A PA; Park, Sung Kyun SK
Publication Date: 2017-11-15

Variant appearance in text: rs7177699
PubMed Link: 29149250
Variant Present in the following documents:
  • Main text
View BVdb publication page



Impact of a Genetic Risk Score for Coronary Artery Disease on Reducing Cardiovascular Risk: A Pilot Randomized Controlled Study.

Frontiers In Cardiovascular Medicine
Knowles, Joshua W JW; Zarafshar, Shirin S; Pavlovic, Aleksandra A; Goldstein, Benjamin A BA; Tsai, Sandra S; Li, Jin J; McConnell, Michael V MV; Absher, Devin D; Ashley, Euan A EA; Kiernan, Michaela M; Ioannidis, John P A JPA; Assimes, Themistocles L TL
Publication Date: 2017

Variant appearance in text: rs7177699
PubMed Link: 28856136
Variant Present in the following documents:
  • Main text
View BVdb publication page



ADAMTS-7 is associated with a high-risk plaque phenotype in human atherosclerosis.

Scientific Reports
Bengtsson, Eva E; Hultman, Karin K; Dunér, Pontus P; Asciutto, Giuseppe G; Almgren, Peter P; Orho-Melander, Marju M; Melander, Olle O; Nilsson, Jan J; Hultgårdh-Nilsson, Anna A; Gonçalves, Isabel I
Publication Date: 2017-06-16

Variant appearance in text: rs7177699
PubMed Link: 28623250
Variant Present in the following documents:
  • Main text
  • 41598_2017_Article_3573.pdf
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Identifying genetic risk variants for coronary heart disease in familial hypercholesterolemia: an extreme genetics approach.

European Journal Of Human Genetics : Ejhg
Versmissen, Jorie J; Oosterveer, Daniëlla M DM; Yazdanpanah, Mojgan M; Dehghan, Abbas A; Hólm, Hilma H; Erdman, Jeanette J; Aulchenko, Yurii S YS; Thorleifsson, Gudmar G; Schunkert, Heribert H; Huijgen, Roeland R; Vongpromek, Ranitha R; Uitterlinden, André G AG; Defesche, Joep C JC; van Duijn, Cornelia M CM; Mulder, Monique M; Dadd, Tony T; Karlsson, Hróbjartur D HD; Ordovas, Jose J; Kindt, Iris I; Jarman, Amelia A; Hofman, Albert A; van Vark-van der Zee, Leonie L; Blommesteijn-Touw, Adriana C AC; Kwekkeboom, Jaap J; Liem, Anho H AH; van der Ouderaa, Frans J FJ; Calandra, Sebastiano S; Bertolini, Stefano S; Averna, Maurizio M; Langslet, Gisle G; Ose, Leiv L; Ros, Emilio E; Almagro, Fátima F; de Leeuw, Peter W PW; Civeira, Fernando F; Masana, Luis L; Pintó, Xavier X; Simoons, Maarten L ML; Schinkel, Arend F L AF; Green, Martin R MR; Zwinderman, Aeilko H AH; Johnson, Keith J KJ; Schaefer, Arne A; Neil, Andrew A; Witteman, Jacqueline C M JC; Humphries, Steve E SE; Kastelein, John J P JJ; Sijbrands, Eric J G EJ
Publication Date: 2015-03

Variant appearance in text: rs7177699
PubMed Link: 24916650
Variant Present in the following documents:
  • Main text
View BVdb publication page



Randomized trial of personal genomics for preventive cardiology: design and challenges.

Circulation. Cardiovascular Genetics
Knowles, Joshua W JW; Assimes, Themistocles L TL; Kiernan, Michaela M; Pavlovic, Aleksandra A; Goldstein, Benjamin A BA; Yank, Veronica V; McConnell, Michael V MV; Absher, Devin D; Bustamante, Carlos C; Ashley, Euan A EA; Ioannidis, John P A JP
Publication Date: 2012-06

Variant appearance in text: rs7177699
PubMed Link: 22715281
Variant Present in the following documents:
  • Main text
View BVdb publication page