ZC3H7B c.582+389T>G

Variant ID: 22-41728620-T-G

NM_017590.5(ZC3H7B):c.582+389T>G

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: rs2143695
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page



The role of AIP variants in pituitary adenomas and concomitant thyroid carcinomas in the Netherlands: a nationwide pathology registry (PALGA) study.

Endocrine
Coopmans, E C EC; Muhammad, A A; Daly, A F AF; de Herder, W W WW; van Kemenade, F J FJ; Beckers, A A; de Haan, M M; van der Lely, A J AJ; Korpershoek, E E; Neggers, S J C M M SJCMM
Publication Date: 2020-06

Variant appearance in text: rs2143695
PubMed Link: 32333269
Variant Present in the following documents:
  • Main text
  • 12020_2020_Article_2303.pdf
View BVdb publication page