NFKB1 c.40-910A>G

Variant ID: 4-103450083-A-G

NM_003998.3(NFKB1):c.40-910A>G

This variant was identified in 4 publications

View GRCh38 version.




Publications:


NFκB1 Polymorphisms Are Associated with Severe Influenza A (H1N1) Virus Infection in a Canadian Population.

Microorganisms
Mirzo, Suhrobjon Mullo SM; Kumar, Anand A; Sharma, Naresh Kumar NK; Li, Lin L; Balshaw, Robert R; Plummer, Francis A FA; Luo, Ma M; Liang, Binhua B
Publication Date: 2022-09-21

Variant appearance in text: rs230533
PubMed Link: 36296162
Variant Present in the following documents:
  • microorganisms-10-01886.pdf
View BVdb publication page



A polygenic risk score predicts mosaic loss of chromosome Y in circulating blood cells.

Cell & Bioscience
Riaz, Moeen M; Mattisson, Jonas J; Polekhina, Galina G; Bakshi, Andrew A; Halvardson, Jonatan J; Danielsson, Marcus M; Ameur, Adam A; McNeil, John J; Forsberg, Lars A LA; Lacaze, Paul P
Publication Date: 2021-12-12

Variant appearance in text: rs230533
PubMed Link: 34895331
Variant Present in the following documents:
  • 13578_2021_716_MOESM1_ESM.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: rs230533
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page



Linkage of Crohn's disease-related serological phenotypes: NFKB1 haplotypes are associated with anti-CBir1 and ASCA, and show reduced NF-kappaB activation.

Gut
Takedatsu, H H; Taylor, K D KD; Mei, L L; McGovern, D P B DP; Landers, C J CJ; Gonsky, R R; Cong, Y Y; Vasiliauskas, E A EA; Ippoliti, A A; Elson, C O CO; Rotter, J I JI; Targan, S R SR
Publication Date: 2009-01

Variant appearance in text: rs230533
PubMed Link: 18832525
Variant Present in the following documents:
  • Main text
View BVdb publication page