FCGR2A c.365-172C>T

Variant ID: 1-161479438-C-T

NM_001136219.1(FCGR2A):c.365-172C>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


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: rs7552317
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page



Genetic risk score predicting risk of rheumatoid arthritis phenotypes and age of symptom onset.

Plos One
Chibnik, Lori B LB; Keenan, Brendan T BT; Cui, Jing J; Liao, Katherine P KP; Costenbader, Karen H KH; Plenge, Robert M RM; Karlson, Elizabeth W EW
Publication Date: 2011

Variant appearance in text: rs7552317
PubMed Link: 21931699
Variant Present in the following documents:
  • Main text
  • pone.0024380.pdf
View BVdb publication page