VCAN c.1042+3285A>G

Variant ID: 5-82811500-A-G

NM_004385.4(VCAN):c.1042+3285A>G

This variant was identified in 15 publications

View GRCh38 version.




Publications:


Association of rare RNF213 variants and intracranial aneurysm risk in a Chinese population.

Annals Of Translational Medicine
Li, Yaqi Y; Liu, Junyu J; Hu, Chongyu C; Luo, Chun C; Zhou, Jilin J; Li, Bingyang B; Liao, Xin X; Liu, Songlin S; Yuan, Dun D; Jiang, Weixi W; Li, Yifeng Y; Yan, Junxia J
Publication Date: 2022-12

Variant appearance in text: rs173686
PubMed Link: 36660619
Variant Present in the following documents:
  • Main text
  • atm-10-24-1336.pdf
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Association of Versican Gene Polymorphisms with Intracranial Aneurysm Susceptibility in the Eastern Chinese Population.

Neuropsychiatric Disease And Treatment
Zhu, Lei L; Yu, Chuanqing C; Zhou, Shuping S; Xue, Min M; Chen, Jie J; Wu, Meijun M; Dong, Shuyang S; Huang, Guanmin G; Chang, Yueyue Y; Zhang, Mei M
Publication Date: 2021

Variant appearance in text: rs173686
PubMed Link: 34908835
Variant Present in the following documents:
  • Main text
  • ndt-17-3531.pdf
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A new Mendelian Randomization method to estimate causal effects of multivariable brain imaging exposures.

Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing
Mo, Chen C; Ye, Zhenyao Z; Ke, Hongjie H; Lu, Tong T; Canida, Travis T; Liu, Song S; Wu, Qiong Q; Zhao, Zhiwei Z; Ma, Yizhou Y; Hong, L Elliot LE; Kochunov, Peter P; Ma, Tianzhou T; Chen, Shuo S
Publication Date: 2022

Variant appearance in text: rs173686
PubMed Link: 34890138
Variant Present in the following documents:
  • Main text
  • nihms-1760600.pdf
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A new Mendelian Randomization method to estimate causal effects of multivariable brain imaging exposures.

Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing
Mo, Chen C; Ye, Zhenyao Z; Ke, Hongjie H; Lu, Tong T; Canida, Travis T; Liu, Song S; Wu, Qiong Q; Zhao, Zhiwei Z; Ma, Yizhou Y; Hong, L Elliot LE; Kochunov, Peter P; Ma, Tianzhou T; Chen, Shuo S
Publication Date: 2022

Variant appearance in text: rs173686
PubMed Link: 34890138
Variant Present in the following documents:
  • Main text
  • nihms-1760600.pdf
View BVdb publication page



The Association between Genes Polymorphisms of Heparan Sulfate Proteoglycan 2 (HSPG2) and Chondroitin Sulfate Proteoglycan 2 (CSPG2) and Intracranial Aneurysm Susceptibility: A Meta-Analysis.

Iranian Journal Of Public Health
Liu, Huahui H; Huang, Wen W
Publication Date: 2019-11

Variant appearance in text: rs173686
PubMed Link: 31970092
Variant Present in the following documents:
  • Main text
  • IJPH-48-1945.pdf
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Data on a genome-wide association study of type 2 diabetes in a Maya population.

Data In Brief
Totomoch-Serra, Armando A; Domínguez-Cruz, Miriam Givisay MG; Muñoz, María de Lourdes ML; García-Escalante, María Guadalupe MG; Burgueño, Juan J; Díaz-Badillo, Álvaro Á; Valadez-González, Nina N; Escalante, Doris Pinto DP
Publication Date: 2020-02

Variant appearance in text: rs173686
PubMed Link: 31872004
Variant Present in the following documents:
  • Main text
View BVdb publication page



Epigenetic landscapes suggest that genetic risk for intracranial aneurysm operates on the endothelium.

Bmc Medical Genomics
Poppenberg, Kerry E KE; Jiang, Kaiyu K; Tso, Michael K MK; Snyder, Kenneth V KV; Siddiqui, Adnan H AH; Kolega, John J; Jarvis, James N JN; Meng, Hui H; Tutino, Vincent M VM
Publication Date: 2019-10-30

Variant appearance in text: rs173686
PubMed Link: 31666072
Variant Present in the following documents:
  • Main text
  • 12920_2019_Article_591.pdf
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Associations among Genetic Variants and Intracranial Aneurysm in a Chinese Population.

Yonsei Medical Journal
Li, Bingyang B; Hu, Chongyu C; Liu, Junyu J; Liao, Xin X; Xun, Jiayu J; Xiao, Manqian M; Yan, Junxia J
Publication Date: 2019-07

Variant appearance in text: rs173686
PubMed Link: 31250579
Variant Present in the following documents:
  • Main text
  • ymj-60-651.pdf
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Genetic Study of White Matter Integrity in UK Biobank (N=8448) and the Overlap With Stroke, Depression, and Dementia.

Stroke
Rutten-Jacobs, Loes C A LCA; Tozer, Daniel J DJ; Duering, Marco M; Malik, Rainer R; Dichgans, Martin M; Markus, Hugh S HS; Traylor, Matthew M
Publication Date: 2018-06

Variant appearance in text: rs173686
PubMed Link: 29752348
Variant Present in the following documents:
  • Main text
  • str-49-1340.pdf
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Population-Wide Genetic Risk Prediction of Complex Diseases: A Pilot Feasibility Study in Macau Population for Precision Public Healthcare Planning.

Scientific Reports
Tsui, Nancy B Y NBY; Cheng, Gregory G; Chung, Teresa T; Lam, Christopher W K CWK; Yee, Anita A; Chung, Peter K C PKC; Kwan, Tsz-Ki TK; Ko, Elaine E; He, Daihai D; Wong, Wing-Tak WT; Lau, Johnson Y N JYN; Lau, Lok Ting LT; Fok, Manson M
Publication Date: 2018-01-30

Variant appearance in text: rs173686
PubMed Link: 29382849
Variant Present in the following documents:
  • 41598_2017_19017_MOESM1_ESM.pdf
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A Novel Association between Lysyl Oxidase Gene Polymorphism and Intracranial Aneurysm in Koreans.

Yonsei Medical Journal
Hong, Eun Pyo EP; Jeon, Jin Pyeong JP; Kim, Sung Eun SE; Yang, Jin Seo JS; Choi, Hyuk Jai HJ; Kang, Suk Hyung SH; Cho, Yong Jun YJ
Publication Date: 2017-09

Variant appearance in text: rs173686
PubMed Link: 28792146
Variant Present in the following documents:
  • Main text
  • ymj-58-1006.pdf
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Admixture Mapping of Subclinical Atherosclerosis and Subsequent Clinical Events Among African Americans in 2 Large Cohort Studies.

Circulation. Cardiovascular Genetics
Shendre, Aditi A; Wiener, Howard H; Irvin, Marguerite R MR; Zhi, Degui D; Limdi, Nita A NA; Overton, Edgar T ET; Wassel, Christina L CL; Divers, Jasmin J; Rotter, Jerome I JI; Post, Wendy S WS; Shrestha, Sadeep S
Publication Date: 2017-04

Variant appearance in text: rs173686
PubMed Link: 28408707
Variant Present in the following documents:
  • Main text
View BVdb publication page



A rare missense variant in RCL1 segregates with depression in extended families.

Molecular Psychiatry
Amin, N N; de Vrij, F M S FMS; Baghdadi, M M; Brouwer, R W W RWW; van Rooij, J G J JGJ; Jovanova, O O; Uitterlinden, A G AG; Hofman, A A; Janssen, H L A HLA; Darwish Murad, S S; Kraaij, R R; Stedehouder, J J; van den Hout, M C G N MCGN; Kros, J M JM; van IJcken, W F J WFJ; Tiemeier, H H; Kushner, S A SA; van Duijn, C M CM
Publication Date: 2018-05

Variant appearance in text: rs173686
PubMed Link: 28322274
Variant Present in the following documents:
  • Main text
  • mp201749a.pdf
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Association of Versican (VCAN) gene polymorphisms rs251124 and rs2287926 (G428D), with intracranial aneurysm.

Meta Gene
Sathyan, Sanish S; Koshy, Linda V LV; Balan, Shabeesh S; Easwer, H V HV; Premkumar, S S; Nair, Suresh S; Bhattacharya, R N RN; Alapatt, Jacob P JP; Banerjee, Moinak M
Publication Date: 2014-12

Variant appearance in text: rs173686
PubMed Link: 25606449
Variant Present in the following documents:
  • Main text
  • mmc1.pdf
  • main.pdf
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Molecular basis and genetic predisposition to intracranial aneurysm.

Annals Of Medicine
Tromp, Gerard G; Weinsheimer, Shantel S; Ronkainen, Antti A; Kuivaniemi, Helena H
Publication Date: 2014-12

Variant appearance in text: rs173686
PubMed Link: 25117779
Variant Present in the following documents:
  • Main text
  • sann46_597.pdf
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Genetic risk factors for intracranial aneurysms: a meta-analysis in more than 116,000 individuals.

Neurology
Alg, Varinder S VS; Sofat, Reecha R; Houlden, Henry H; Werring, David J DJ
Publication Date: 2013-06-04

Variant appearance in text: rs173686
PubMed Link: 23733552
Variant Present in the following documents:
  • Main text
View BVdb publication page