SREBF2 c.2208+414A>G

Variant ID: 22-42281429-A-G

NM_004599.3(SREBF2):c.2208+414A>G

This variant was identified in 6 publications

View GRCh38 version.




Publications:


Single-nucleotide polymorphisms as important risk factors of diabetes among Middle East population.

Human Genomics
Akhlaghipour, Iman I; Bina, Amir Reza AR; Mogharrabi, Mohammad Reza MR; Fanoodi, Ali A; Ebrahimian, Amir Reza AR; Khojasteh Kaffash, Soroush S; Babazadeh Baghan, Atefeh A; Khorashadizadeh, Mohammad Erfan ME; Taghehchian, Negin N; Moghbeli, Meysam M
Publication Date: 2022-04-02

Variant appearance in text: rs1052717
PubMed Link: 35366956
Variant Present in the following documents:
  • Main text
View BVdb publication page



Associations of the SREBF2 Gene and INSIG2 Polymorphisms with Obesity and Dyslipidemia in Thai Psychotic Disorder Patients Treated with Risperidone.

Journal Of Personalized Medicine
Vanwong, Natchaya N; Sukasem, Chonlaphat C; Unaharassamee, Weerapon W; Jiratjintana, Napa N; Na Nakorn, Chalitpon C; Hongkaew, Yaowaluck Y; Puangpetch, Apichaya A
Publication Date: 2021-09-22

Variant appearance in text: rs1052717
PubMed Link: 34683084
Variant Present in the following documents:
  • Main text
  • jpm-11-00943.pdf
View BVdb publication page



Pharmacogenetics of Antipsychotic Drug Treatment: Update and Clinical Implications.

Molecular Neuropsychiatry
Yoshida, Kazunari K; Müller, Daniel J DJ
Publication Date: 2020-04

Variant appearance in text: rs1052717
PubMed Link: 32399466
Variant Present in the following documents:
  • Main text
View BVdb publication page



Non-CYP2D6 Variants Selected by a GWAS Improve the Prediction of Impaired Tamoxifen Metabolism in Patients with Breast Cancer.

Journal Of Clinical Medicine
Hennig, Ewa E EE; Piątkowska, Magdalena M; Goryca, Krzysztof K; Pośpiech, Ewelina E; Paziewska, Agnieszka A; Karczmarski, Jakub J; Kluska, Anna A; Brewczyńska, Elżbieta E; Ostrowski, Jerzy J
Publication Date: 2019-07-24

Variant appearance in text: rs1052717
PubMed Link: 31344832
Variant Present in the following documents:
  • Main text
  • jcm-08-01087.pdf
View BVdb publication page



Association of genetic variations in the lipid regulatory pathway genes FBXW7 and SREBPs with coronary artery disease among Han Chinese and Uygur Chinese populations in Xinjiang, China.

Oncotarget
Abudesimu, Asiya A; Adi, Dilare D; Siti, Dilixiati D; Xie, Xiang X; Yang, Yi-Ning YN; Li, Xiao-Mei XM; Wang, Ying-Hong YH; Wang, Yong-Tao YT; Meng, Ya-Jie YJ; Liu, Fen F; Chen, Bang-Dang BD; Ma, Xiang X; Fu, Zhen-Yan ZY; Ma, Yi-Tong YT
Publication Date: 2017-10-20

Variant appearance in text: rs1052717
PubMed Link: 29152152
Variant Present in the following documents:
  • Main text
  • oncotarget-08-88199.pdf
View BVdb publication page



Significant association of SREBP-2 genetic polymorphisms with avascular necrosis in the Korean population.

Bmc Medical Genetics
Kim, Tae-Ho TH; Baek, Jeong-In JI; Hong, Jung Min JM; Choi, Su-Jin SJ; Lee, Hye-Jin HJ; Cho, Hyun-Ju HJ; Park, Eui Kyun EK; Kim, Un-Kyung UK; Kim, Shin-Yoon SY
Publication Date: 2008-10-27

Variant appearance in text: rs1052717
PubMed Link: 18954446
Variant Present in the following documents:
  • Main text
  • 1471-2350-9-94.pdf
View BVdb publication page