IFNGR1 c.86-4992C>T

Variant ID: 6-137533206-G-A

NM_000416.2(IFNGR1):c.86-4992C>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Biomarkers associated with the development of comorbidities in patients with atopic dermatitis: a systematic review.

Allergy
Broderick, Conor C; Ziehfreund, Stefanie S; van Bart, Karin K; Arents, Bernd B; Eyerich, Kilian K; Weidinger, Stephan S; Rastrick, Joseph J; Zink, Alexander A; Flohr, Carsten C; ,
Publication Date: 2022-11-10

Variant appearance in text: rs17175127
PubMed Link: 36366871
Variant Present in the following documents:
  • Main text
  • ALL-78-84.pdf
View BVdb publication page



Targeted deep sequencing identifies rare loss-of-function variants in IFNGR1 for risk of atopic dermatitis complicated by eczema herpeticum.

The Journal Of Allergy And Clinical Immunology
Gao, Li L; Bin, Lianghua L; Rafaels, Nicholas M NM; Huang, Lili L; Potee, Joseph J; Ruczinski, Ingo I; Beaty, Terri H TH; Paller, Amy S AS; Schneider, Lynda C LC; Gallo, Rich R; Hanifin, Jon M JM; Beck, Lisa A LA; Geha, Raif S RS; Mathias, Rasika A RA; Barnes, Kathleen C KC; Leung, Donald Y M DYM
Publication Date: 2015-12

Variant appearance in text: rs17175127
PubMed Link: 26343451
Variant Present in the following documents:
  • Main text
View BVdb publication page