STARD3 c.-51-2036A>C

Variant ID: 17-37807698-A-C

NM_006804.3(STARD3):c.-51-2036A>C

This variant was identified in 9 publications

View GRCh38 version.




Publications:


ASO Author Reflections: From Susceptibility Loci to Oncologically Relevant SNPs in Upper Gastrointestinal Cancer.

Annals Of Surgical Oncology
Jung, Jin-On JO; Bruns, Christiane J CJ; Schmidt, Thomas T
Publication Date: 2022-02

Variant appearance in text: rs9972882
PubMed Link: 34591224
Variant Present in the following documents:
  • Main text
  • 10434_2021_Article_10819.pdf
View BVdb publication page



ASO Author Reflections: From Susceptibility Loci to Oncologically Relevant SNPs in Upper Gastrointestinal Cancer.

Annals Of Surgical Oncology
Jung, Jin-On JO; Bruns, Christiane J CJ; Schmidt, Thomas T
Publication Date: 2021-09-30

Variant appearance in text: rs9972882
PubMed Link: 34591224
Variant Present in the following documents:
  • Main text
  • 10434_2021_Article_10819.pdf
View BVdb publication page



Clinical Relevance of Gastroesophageal Cancer Associated SNPs for Oncologic Outcome After Curative Surgery.

Annals Of Surgical Oncology
Jung, Jin-On JO; Wirsik, Naita Maren NM; Nienhüser, Henrik H; Peters, Leila L; Müller-Stich, Beat Peter BP; Hess, Timo T; Schüller, Vitalia V; Schumacher, Johannes J; Schmidt, Thomas T
Publication Date: 2022-02

Variant appearance in text: rs9972882
PubMed Link: 34529172
Variant Present in the following documents:
  • Main text
  • 10434_2021_Article_10771.pdf
View BVdb publication page



Clinical Relevance of Gastroesophageal Cancer Associated SNPs for Oncologic Outcome After Curative Surgery.

Annals Of Surgical Oncology
Jung, Jin-On JO; Wirsik, Naita Maren NM; Nienhüser, Henrik H; Peters, Leila L; Müller-Stich, Beat Peter BP; Hess, Timo T; Schüller, Vitalia V; Schumacher, Johannes J; Schmidt, Thomas T
Publication Date: 2021-09-16

Variant appearance in text: rs9972882
PubMed Link: 34529172
Variant Present in the following documents:
  • Main text
  • 10434_2021_Article_10771.pdf
View BVdb publication page



Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population.

Human Genetics
Hebbar, Prashantha P; Abubaker, Jehad Ahmed JA; Abu-Farha, Mohamed M; Alsmadi, Osama O; Elkum, Naser N; Alkayal, Fadi F; John, Sumi Elsa SE; Channanath, Arshad A; Iqbal, Rasheeba R; Pitkaniemi, Janne J; Tuomilehto, Jaakko J; Sladek, Robert R; Al-Mulla, Fahd F; Thanaraj, Thangavel Alphonse TA
Publication Date: 2021-03

Variant appearance in text: rs9972882
PubMed Link: 32902719
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association study identifies novel risk variants from RPS6KA1, CADPS, VARS, and DHX58 for fasting plasma glucose in Arab population.

Scientific Reports
Hebbar, Prashantha P; Abu-Farha, Mohamed M; Alkayal, Fadi F; Nizam, Rasheeba R; Elkum, Naser N; Melhem, Motasem M; John, Sumi Elsa SE; Channanath, Arshad A; Abubaker, Jehad J; Bennakhi, Abdullah A; Al-Ozairi, Ebaa E; Tuomilehto, Jaakko J; Pitkaniemi, Janne J; Alsmadi, Osama O; Al-Mulla, Fahd F; Thanaraj, Thangavel Alphonse TA
Publication Date: 2020-01-13

Variant appearance in text: rs9972882
PubMed Link: 31932636
Variant Present in the following documents:
  • Main text
  • 41598_2019_Article_57072.pdf
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A Perception on Genome-Wide Genetic Analysis of Metabolic Traits in Arab Populations.

Frontiers In Endocrinology
Hebbar, Prashantha P; Abubaker, Jehad Ahmed JA; Abu-Farha, Mohamed M; Tuomilehto, Jaakko J; Al-Mulla, Fahd F; Thanaraj, Thangavel Alphonse TA
Publication Date: 2019

Variant appearance in text: rs9972882
PubMed Link: 30761081
Variant Present in the following documents:
  • Main text
  • fendo-10-00008.pdf
View BVdb publication page



Clinical Implication and the Hereditary Factors of NM23 in Hepatocellular Carcinoma Based on Bioinformatics Analysis and Genome-Wide Association Study.

Journal Of Oncology
Yang, Chengkun C; Han, Chuangye C; Wang, Xiangkun X; Liao, Xiwen X; Liu, Xiaoguang X; Qin, Wei W; Yu, Long L; Zhu, Guangzhi G; Su, Hao H; Lu, Sicong S; Chen, Zhiwei Z; Yu, Tingdong T; Liu, Zhen Z; Huang, Ketuan K; Liu, Zhengtao Z; Liang, Yu Y; Huang, Jianlu J; Peng, Tao T
Publication Date: 2018

Variant appearance in text: rs9972882
PubMed Link: 30662464
Variant Present in the following documents:
  • Main text
  • JO2018-6594169.pdf
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Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population.

Journal Of Lipid Research
Hebbar, Prashantha P; Nizam, Rasheeba R; Melhem, Motasem M; Alkayal, Fadi F; Elkum, Naser N; John, Sumi Elsa SE; Tuomilehto, Jaakko J; Alsmadi, Osama O; Thanaraj, Thangavel Alphonse TA
Publication Date: 2018-10

Variant appearance in text: rs9972882
PubMed Link: 30108155
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide analysis of the genetic regulation of gene expression in human neutrophils.

Nature Communications
Andiappan, Anand Kumar AK; Melchiotti, Rossella R; Poh, Tuang Yeow TY; Nah, Michelle M; Puan, Kia Joo KJ; Vigano, Elena E; Haase, Doreen D; Yusof, Nurhashikin N; San Luis, Boris B; Lum, Josephine J; Kumar, Dilip D; Foo, Shihui S; Zhuang, Li L; Vasudev, Anusha A; Irwanto, Astrid A; Lee, Bernett B; Nardin, Alessandra A; Liu, Hong H; Zhang, Furen F; Connolly, John J; Liu, Jianjun J; Mortellaro, Alessandra A; Wang, De Yun Y; Poidinger, Michael M; Larbi, Anis A; Zolezzi, Francesca F; Rotzschke, Olaf O
Publication Date: 2015-08-10

Variant appearance in text: rs9972882
PubMed Link: 26259071
Variant Present in the following documents:
  • ncomms8971-s1.pdf
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Gender-stratified gene and gene-treatment interactions in smoking cessation.

The Pharmacogenomics Journal
Lee, W W; Bergen, A W AW; Swan, G E GE; Li, D D; Liu, J J; Thomas, P P; Tyndale, R F RF; Benowitz, N L NL; Lerman, C C; Conti, D V DV
Publication Date: 2012-12

Variant appearance in text: rs9972882
PubMed Link: 21808284
Variant Present in the following documents:
  • NIHMS305090-supplement-3.pdf
View BVdb publication page