HLA-DRA c.*163T>G

Variant ID: 6-32412580-T-G

NM_019111.4(HLA-DRA):c.*163T>G

This variant was identified in 9 publications

View GRCh38 version.




Publications:


Sex differences in the genetics of sarcoidosis across European and African ancestry populations.

Frontiers In Medicine
Xiong, Ying Y; Kullberg, Susanna S; Garman, Lori L; Pezant, Nathan N; Ellinghaus, David D; Vasila, Vasiliki V; Eklund, Anders A; Rybicki, Benjamin A BA; Iannuzzi, Michael C MC; Schreiber, Stefan S; Müller-Quernheim, Joachim J; Montgomery, Courtney G CG; Grunewald, Johan J; Padyukov, Leonid L; Rivera, Natalia V NV
Publication Date: 2023

Variant appearance in text: rs7197
PubMed Link: 37250650
Variant Present in the following documents:
  • Main text
  • fmed-10-1132799.pdf
View BVdb publication page



Molecular Mechanisms in Autoimmune Thyroid Disease.

Cells
Vargas-Uricoechea, Hernando H
Publication Date: 2023-03-16

Variant appearance in text: rs7197
PubMed Link: 36980259
Variant Present in the following documents:
  • Main text
  • cells-12-00918.pdf
View BVdb publication page



Genetics and epigenetics of primary Sjögren syndrome: implications for future therapies.

Nature Reviews. Rheumatology
Thorlacius, Gudny Ella GE; Björk, Albin A; Wahren-Herlenius, Marie M
Publication Date: 2023-03-13

Variant appearance in text: rs7197
PubMed Link: 36914790
Variant Present in the following documents:
  • Main text
  • 41584_2023_Article_932.pdf
View BVdb publication page



HLA-DRA Gene Polymorphisms Are Associated with Graves' Disease as an Autoimmune Thyroid Disease.

Biomed Research International
Du, Peng P; Zhu, Jiaoli J; Yao, Qiuming Q; Cai, Tiantian T; Xu, Jianbin J; Fang, Yudie Y; Wu, Yuqing Y; Zhang, Wen W; Zhang, Jin-An JA
Publication Date: 2022

Variant appearance in text: rs7197
PubMed Link: 36132072
Variant Present in the following documents:
  • BMRI2022-6839634.pdf
View BVdb publication page



Identification of host-pathogen-disease relationships using a scalable multiplex serology platform in UK Biobank.

Nature Communications
Mentzer, Alexander J AJ; Brenner, Nicole N; Allen, Naomi N; Littlejohns, Thomas J TJ; Chong, Amanda Y AY; Cortes, Adrian A; Almond, Rachael R; Hill, Michael M; Sheard, Simon S; McVean, Gil G; , ; Collins, Rory R; Hill, Adrian V S AVS; Waterboer, Tim T
Publication Date: 2022-04-05

Variant appearance in text: rs7197
PubMed Link: 35383168
Variant Present in the following documents:
  • Main text
  • 41467_2022_Article_29307.pdf
View BVdb publication page



Genetic variation in cervical preinvasive and invasive disease: a genome-wide association study.

The Lancet. Oncology
Bowden, Sarah J SJ; Bodinier, Barbara B; Kalliala, Ilkka I; Zuber, Verena V; Vuckovic, Dragana D; Doulgeraki, Triada T; Whitaker, Matthew D MD; Wielscher, Matthias M; Cartwright, Rufus R; Tsilidis, Konstantinos K KK; Bennett, Phillip P; Jarvelin, Marjo-Riitta MR; Flanagan, James M JM; Chadeau-Hyam, Marc M; Kyrgiou, Maria M; ,
Publication Date: 2021-04

Variant appearance in text: rs7197
PubMed Link: 33794208
Variant Present in the following documents:
  • mmc1.pdf
View BVdb publication page



Analysis of Single Nucleotide Polymorphisms in HLA-DRA, IL2RA , and HMGB1 Genes in Multiple Sclerosis.

Reports Of Biochemistry & Molecular Biology
Asouri, Mohsen M; Alinejad Rokni, Hamid H; Sahraian, Mohammad Ali MA; Fattahi, Sadegh S; Motamed, Nima N; Doosti, Rozita R; Rahimi, Hamzeh H; Lotfi, Maryam M; Moslemi, Azam A; Karimpoor, Morteza M; Mahboudi, Fereidoun F; Akhavan-Niaki, Haleh H
Publication Date: 2020-07

Variant appearance in text: rs7197
PubMed Link: 33178870
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of HLA-DRA and IL2RA Polymorphisms with the Severity and Relapses Rate of Multiple Sclerosis in an Iranian Population.

Reports Of Biochemistry & Molecular Biology
Asouri, Mohsen M; Alinejad Rokni, Hamid H; Sahraian, Mohammad Ali MA; Fattahi, Sadegh S; Motamed, Nima N; Doosti, Rozita R; Amirbozorgi, Galia G; Karimpoor, Morteza M; Mahboudi, Fereidoun F; Akhavan-Niaki, Haleh H
Publication Date: 2020-07

Variant appearance in text: rs7197
PubMed Link: 33178861
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic and clinical basis for two distinct subtypes of primary Sjögren's syndrome.

Rheumatology (Oxford, England)
Thorlacius, Guðný Ella GE; Hultin-Rosenberg, Lina L; Sandling, Johanna K JK; Bianchi, Matteo M; Imgenberg-Kreuz, Juliana J; Pucholt, Pascal P; Theander, Elke E; Kvarnström, Marika M; Forsblad-d'Elia, Helena H; Bucher, Sara Magnusson SM; Norheim, Katrine B KB; Johnsen, Svein Joar Auglænd SJA; Hammenfors, Daniel D; Skarstein, Kathrine K; Jonsson, Malin V MV; Baecklund, Eva E; Aqrawi, Lara A LA; Jensen, Janicke Liaaen JL; Palm, Øyvind Ø; Morris, Andrew P AP; , ; , ; Meadows, Jennifer R S JRS; Rantapää-Dahlqvist, Solbritt S; Mandl, Thomas T; Eriksson, Per P; Lind, Lars L; Omdal, Roald R; Jonsson, Roland R; Lindblad-Toh, Kerstin K; Rönnblom, Lars L; Wahren-Herlenius, Marie M; Nordmark, Gunnel G
Publication Date: 2021-02-01

Variant appearance in text: rs7197
PubMed Link: 32889544
Variant Present in the following documents:
  • Main text
  • keaa367.pdf
View BVdb publication page