BCL2L11 c.498+5332T>C

Variant ID: 2-111913056-T-C

NM_138621.4(BCL2L11):c.498+5332T>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genetic feature engineering enables characterisation of shared risk factors in immune-mediated diseases.

Genome Medicine
Burren, Oliver S OS; Reales, Guillermo G; Wong, Limy L; Bowes, John J; Lee, James C JC; Barton, Anne A; Lyons, Paul A PA; Smith, Kenneth G C KGC; Thomson, Wendy W; Kirk, Paul D W PDW; Wallace, Chris C
Publication Date: 2020-11-25

Variant appearance in text: rs13405741
PubMed Link: 33239102
Variant Present in the following documents:
  • Main text
  • 13073_2020_Article_797.pdf
View BVdb publication page



Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs.

Jci Insight
Chen, Xiao-Feng XF; Guo, Ming-Rui MR; Duan, Yuan-Yuan YY; Jiang, Feng F; Wu, Hao H; Dong, Shan-Shan SS; Zhou, Xiao-Rong XR; Thynn, Hlaing Nwe HN; Liu, Cong-Cong CC; Zhang, Lin L; Guo, Yan Y; Yang, Tie-Lin TL
Publication Date: 2020-09-03

Variant appearance in text: rs13405741
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page