ALDH3B1 c.1111-463T>C

Variant ID: 11-67793014-T-C

NM_000694.4(ALDH3B1):c.1111-463T>C

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Genetic variations in olfactory receptor gene OR2AG2 in a large multigenerational family with asthma.

Scientific Reports
Chakraborty, Samarpana S; Dakle, Pushkar P; Sinha, Anirban A; Vishweswaraiah, Sangeetha S; Nagori, Aditya A; Salimath, Shivalingaswamy S; Prakash, Y S YS; Lodha, R R; Kabra, S K SK; Ghosh, Balaram B; Faruq, Mohammed M; Mahesh, P A PA; Agrawal, Anurag A
Publication Date: 2019-12-13

Variant appearance in text: rs105147
PubMed Link: 31836740
Variant Present in the following documents:
  • 41598_2019_54718_MOESM1_ESM.pdf
View BVdb publication page



Do nuclear-encoded core subunits of mitochondrial complex I confer genetic susceptibility to schizophrenia in Han Chinese populations?

Scientific Reports
Li, Xiao X; Zhang, Wen W; Tang, Jinsong J; Tan, Liwen L; Luo, Xiong-jian XJ; Chen, Xiaogang X; Yao, Yong-Gang YG
Publication Date: 2015-06-08

Variant appearance in text: rs105147
PubMed Link: 26053550
Variant Present in the following documents:
  • Main text
  • srep11076.pdf
View BVdb publication page



Genetic variants in RKIP are associated with clear cell renal cell carcinoma risk in a Chinese population.

Plos One
Cao, Qiang Q; Wang, Jian J; Zhang, Mingcong M; Li, Pu P; Qian, Jian J; Zhang, Shaobo S; Zhang, Lei L; Ju, Xiaobing X; Wang, Meilin M; Zhang, Zhengdong Z; Li, Jie J; Gu, Min M; Zhang, Wei W; Qin, Chao C; Shao, Pengfei P; Yin, Changjun C
Publication Date: 2014

Variant appearance in text: rs105147
PubMed Link: 25329396
Variant Present in the following documents:
  • Main text
  • pone.0109285.pdf
View BVdb publication page



Admixture mapping and subsequent fine-mapping suggests a biologically relevant and novel association on chromosome 11 for type 2 diabetes in African Americans.

Plos One
Jeff, Janina M JM; Armstrong, Loren L LL; Ritchie, Marylyn D MD; Denny, Joshua C JC; Kho, Abel N AN; Basford, Melissa A MA; Wolf, Wendy A WA; Pacheco, Jennifer A JA; Li, Rongling R; Chisholm, Rex L RL; Roden, Dan M DM; Hayes, M Geoffrey MG; Crawford, Dana C DC
Publication Date: 2014

Variant appearance in text: rs105147
PubMed Link: 24595071
Variant Present in the following documents:
  • Main text
  • pone.0086931.pdf
View BVdb publication page



Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample.

American Journal Of Human Genetics
Suarez, Brian K BK; Duan, Jubao J; Sanders, Alan R AR; Hinrichs, Anthony L AL; Jin, Carol H CH; Hou, Cuiping C; Buccola, Nancy G NG; Hale, Nancy N; Weilbaecher, Ann N AN; Nertney, Deborah A DA; Olincy, Ann A; Green, Susan S; Schaffer, Arthur W AW; Smith, Christopher J CJ; Hannah, Dominique E DE; Rice, John P JP; Cox, Nancy J NJ; Martinez, Maria M; Mowry, Bryan J BJ; Amin, Farooq F; Silverman, Jeremy M JM; Black, Donald W DW; Byerley, William F WF; Crowe, Raymond R RR; Freedman, Robert R; Cloninger, C Robert CR; Levinson, Douglas F DF; Gejman, Pablo V PV
Publication Date: 2006-02

Variant appearance in text: rs105147
PubMed Link: 16400611
Variant Present in the following documents:
  • Main text
View BVdb publication page