TNFSF8 c.310+665A>G

Variant ID: 9-117667443-T-C

NM_001244.3(TNFSF8):c.310+665A>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Associations between TNFSF4, TNFSF8 and TNFSF15 and Behçet's disease but not VKH syndrome in Han Chinese.

Oncotarget
Jiang, Yan Y; Cheng, Ling L; Li, Xin X; Zhou, Wenke W; Zhang, Li L
Publication Date: 2017-12-01

Variant appearance in text: rs3181362
PubMed Link: 29285231
Variant Present in the following documents:
  • Main text
  • oncotarget-08-105037.pdf
View BVdb publication page



Genome-wide SNP typing reveals signatures of population history.

Genomics
Hughes, Austin L AL; Welch, Robert R; Puri, Vinita V; Matthews, Casey C; Haque, Kashif K; Chanock, Stephen J SJ; Yeager, Meredith M
Publication Date: 2008-07

Variant appearance in text: rs3181362
PubMed Link: 18485661
Variant Present in the following documents:
  • Main text
View BVdb publication page