TNFSF11 c.388-1690T>C

Variant ID: 13-43173198-T-C

NM_003701.3(TNFSF11):c.388-1690T>C

This variant was identified in 6 publications

View GRCh38 version.




Publications:


Genetic Mutations in TNFSF11 Were Associated With the Chronicity of Hepatitis C Among Chinese Han Population.

Frontiers In Medicine
Huang, Peng P; Hou, Yu-Qing YQ; Wu, Jing-Jing JJ; Wang, Yi-Di YD; Ye, Xiang-Yu XY; Zang, Feng F; Yu, Rong-Bin RB; Yang, Sheng S
Publication Date: 2021

Variant appearance in text: rs3742257
PubMed Link: 34660648
Variant Present in the following documents:
  • Main text
  • fmed-08-743406.pdf
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Polymorphisms of CSF1 and TM7SF4 genes in a case of mild juvenile Paget's disease found using next-generation sequencing.

Croatian Medical Journal
Donáth, Judit J; Speer, Gábor G; Kósa, János P JP; Árvai, Kristóf K; Balla, Bernadett B; Juhász, Péter P; Lakatos, Péter P; Poór, Gyula G
Publication Date: 2015-04

Variant appearance in text: rs3742257
PubMed Link: 25891874
Variant Present in the following documents:
  • Main text
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Moyamoya disease and syndromes: from genetics to clinical management.

The Application Of Clinical Genetics
Guey, Stéphanie S; Tournier-Lasserve, Elisabeth E; Hervé, Dominique D; Kossorotoff, Manoelle M
Publication Date: 2015

Variant appearance in text: rs3742257
PubMed Link: 25733922
Variant Present in the following documents:
  • Main text
  • tacg-8-049.pdf
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TNFRSF11A and TNFSF11 are associated with age at menarche and natural menopause in white women.

Menopause (New York, N.Y.)
Lu, Yan Y; Liu, Pengyuan P; Recker, Robert R RR; Deng, Hong-Wen HW; Dvornyk, Volodymyr V
Publication Date: 2010

Variant appearance in text: rs3742257
PubMed Link: 20531232
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association analyses of RANKL/RANK/OPG gene polymorphisms with femoral neck compression strength index variation in Caucasians.

Calcified Tissue International
Dong, Shan-Shan SS; Liu, Xiao-Gang XG; Chen, Yuan Y; Guo, Yan Y; Wang, Liang L; Zhao, Jian J; Xiong, Dong-Hai DH; Xu, Xiang-Hong XH; Recker, Robert R RR; Deng, Hong-Wen HW
Publication Date: 2009-08

Variant appearance in text: rs3742257
PubMed Link: 19458885
Variant Present in the following documents:
  • Main text
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Robust and comprehensive analysis of 20 osteoporosis candidate genes by very high-density single-nucleotide polymorphism screen among 405 white nuclear families identified significant association and gene-gene interaction.

Journal Of Bone And Mineral Research : The Official Journal Of The American Society For Bone And Mineral Research
Xiong, Dong-Hai DH; Shen, Hui H; Zhao, Lan-Juan LJ; Xiao, Peng P; Yang, Tie-Lin TL; Guo, Yan Y; Wang, Wei W; Guo, Yan-Fang YF; Liu, Yong-Jun YJ; Recker, Robert R RR; Deng, Hong-Wen HW
Publication Date: 2006-11

Variant appearance in text: rs3742257
PubMed Link: 17002564
Variant Present in the following documents:
  • Main text
View BVdb publication page