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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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