HLA-DRA c.611-10T>C

Variant ID: 6-32411523-T-C

NM_019111.4(HLA-DRA):c.611-10T>C

This variant was identified in 16 publications

View GRCh38 version.




Publications:


Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: rs2239804
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



MHC Variants Associated With Symptomatic Versus Asymptomatic SARS-CoV-2 Infection in Highly Exposed Individuals.

Frontiers In Immunology
Castelli, Erick C EC; de Castro, Mateus V MV; Naslavsky, Michel S MS; Scliar, Marilia O MO; Silva, Nayane S B NSB; Andrade, Heloisa S HS; Souza, Andreia S AS; Pereira, Raphaela N RN; Castro, Camila F B CFB; Mendes-Junior, Celso T CT; Meyer, Diogo D; Nunes, Kelly K; Matos, Larissa R B LRB; Silva, Monize V R MVR; Wang, Jaqueline Y T JYT; Esposito, Joyce J; Coria, Vivian R VR; Bortolin, Raul H RH; Hirata, Mario H MH; Magawa, Jhosiene Y JY; Cunha-Neto, Edecio E; Coelho, Verônica V; Santos, Keity S KS; Marin, Maria Lucia C MLC; Kalil, Jorge J; Mitne-Neto, Miguel M; Maciel, Rui M B RMB; Passos-Bueno, Maria Rita MR; Zatz, Mayana M
Publication Date: 2021

Variant appearance in text: rs2239804
PubMed Link: 34650566
Variant Present in the following documents:
  • Table_3.xlsx, sheet 2
  • Table_3.xlsx, sheet 4
  • Table_3.xlsx, sheet 3
  • Table_3.xlsx, sheet 1
  • Table_3.xlsx, sheet 5
View BVdb publication page



Disseminated Talaromyces marneffei Infection in a Non-HIV Infant With a Homozygous Private Variant of RELB.

Frontiers In Cellular And Infection Microbiology
Ding, Xiaofang X; Huang, Han H; Zhong, Lili L; Chen, Min M; Peng, Fang F; Zhang, Bing B; Cui, Xinyu X; Yang, Xiu-An XA
Publication Date: 2021

Variant appearance in text: rs2239804
PubMed Link: 33791233
Variant Present in the following documents:
  • Table_2.xlsx, sheet 1
View BVdb publication page



Identification of trans-eQTLs using mediation analysis with multiple mediators.

Bmc Bioinformatics
Shan, Nayang N; Wang, Zuoheng Z; Hou, Lin L
Publication Date: 2019-03-29

Variant appearance in text: rs2239804
PubMed Link: 30925861
Variant Present in the following documents:
  • Main text
  • 12859_2019_Article_2651.pdf
View BVdb publication page



Genome-wide scans of myopia in Pennsylvania Amish families reveal significant linkage to 12q15, 8q21.3 and 5p15.33.

Human Genetics
Musolf, Anthony M AM; Simpson, Claire L CL; Alexander, Theresa A TA; Portas, Laura L; Murgia, Federico F; Ciner, Elise B EB; Stambolian, Dwight D; Bailey-Wilson, Joan E JE
Publication Date: 2019-04

Variant appearance in text: rs2239804
PubMed Link: 30826882
Variant Present in the following documents:
  • Main text
View BVdb publication page



Fine-mapping of HLA class I and class II genes identified two independent novel variants associated with nasopharyngeal carcinoma susceptibility.

Cancer Medicine
Wang, Tong-Min TM; Zhou, Ting T; He, Yong-Qiao YQ; Xue, Wen-Qiong WQ; Zhang, Jiang-Bo JB; Zheng, Xiao-Hui XH; Li, Xi-Zhao XZ; Zhang, Shao-Dan SD; Zeng, Yi-Xin YX; Jia, Wei-Hua WH
Publication Date: 2018-12

Variant appearance in text: rs2239804
PubMed Link: 30378292
Variant Present in the following documents:
  • CAM4-7-6308-s006.xlsx, sheet 1
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: HLA-DRA: 611-10T>C; rs2239804
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_5.xlsx, sheet 1
  • Table_7.xlsx, sheet 1
  • Table_6.xlsx, sheet 1
View BVdb publication page



Genome-wide association study of antisocial personality disorder.

Translational Psychiatry
Rautiainen, M-R MR; Paunio, T T; Repo-Tiihonen, E E; Virkkunen, M M; Ollila, H M HM; Sulkava, S S; Jolanki, O O; Palotie, A A; Tiihonen, J J
Publication Date: 2016-09-06

Variant appearance in text: rs2239804
PubMed Link: 27598967
Variant Present in the following documents:
  • Main text
  • tp2016155a.pdf
View BVdb publication page



Efficient generalized least squares method for mixed population and family-based samples in genome-wide association studies.

Genetic Epidemiology
Li, Jia J; Yang, James J; Levin, Albert M AM; Montgomery, Courtney G CG; Datta, Indrani I; Trudeau, Sheri S; Adrianto, Indra I; McKeigue, Paul P; Iannuzzi, Michael C MC; Rybicki, Benjamin A BA
Publication Date: 2014-07

Variant appearance in text: rs2239804
PubMed Link: 24845555
Variant Present in the following documents:
  • Main text
View BVdb publication page



Host genetics and immune control of HIV-1 infection: fine mapping for the extended human MHC region in an African cohort.

Genes And Immunity
Prentice, H A HA; Pajewski, N M NM; He, D D; Zhang, K K; Brown, E E EE; Kilembe, W W; Allen, S S; Hunter, E E; Kaslow, R A RA; Tang, J J
Publication Date: 2014

Variant appearance in text: rs2239804
PubMed Link: 24784026
Variant Present in the following documents:
  • NIHMS580846-supplement-1.xlsx, sheet 2
  • NIHMS580846-supplement-1.xlsx, sheet 3
View BVdb publication page



Single nucleotide polymorphism (SNP)-strings: an alternative method for assessing genetic associations.

Plos One
Goodin, Douglas S DS; Khankhanian, Pouya P
Publication Date: 2014

Variant appearance in text: rs2239804
PubMed Link: 24727690
Variant Present in the following documents:
  • Main text
  • pone.0090034.pdf
View BVdb publication page



Diversity of extended HLA-DRB1 haplotypes in the Finnish population.

Plos One
Wennerström, Annika A; Vlachopoulou, Efthymia E; Lahtela, L Elisa LE; Paakkanen, Riitta R; Eronen, Katja T KT; Seppänen, Mikko M; Lokki, Marja-Liisa ML
Publication Date: 2013

Variant appearance in text: rs2239804
PubMed Link: 24278156
Variant Present in the following documents:
  • Main text
  • pone.0079690.pdf
View BVdb publication page



Genome-wide association study of asthma identifies RAD50-IL13 and HLA-DR/DQ regions.

The Journal Of Allergy And Clinical Immunology
Li, Xingnan X; Howard, Timothy D TD; Zheng, Siqun L SL; Haselkorn, Tmirah T; Peters, Stephen P SP; Meyers, Deborah A DA; Bleecker, Eugene R ER
Publication Date: 2010-02

Variant appearance in text: rs2239804
PubMed Link: 20159242
Variant Present in the following documents:
  • Main text
View BVdb publication page



Detecting significant single-nucleotide polymorphisms in a rheumatoid arthritis study using random forests.

Bmc Proceedings
Wang, Minghui M; Chen, Xiang X; Zhang, Meizhuo M; Zhu, Wensheng W; Cho, Kelly K; Zhang, Heping H
Publication Date: 2009-12-15

Variant appearance in text: rs2239804
PubMed Link: 20018063
Variant Present in the following documents:
  • Main text
  • 1753-6561-3-S7-S69.pdf
View BVdb publication page



Haplotype-based search for SNPs associated with differential type 1 diabetes risk among chromosomes carrying a specific HLA DRB1-DQA1-DQB1 haplotype.

Diabetes, Obesity & Metabolism
McGinnis, R R; McLaren, W W; Ranganath, V V; Whittaker, P P; Hunt, S S; Deloukas, P P; ,
Publication Date: 2009-02

Variant appearance in text: rs2239804
PubMed Link: 19143810
Variant Present in the following documents:
  • Main text
View BVdb publication page



Variable selection in logistic regression for detecting SNP-SNP interactions: the rheumatoid arthritis example.

European Journal Of Human Genetics : Ejhg
Lin, Hui-Yi HY; Desmond, Renee R; Bridges, S Louis SL; Soong, Seng-jaw SJ
Publication Date: 2008-06

Variant appearance in text: rs2239804
PubMed Link: 18231122
Variant Present in the following documents:
  • Main text
View BVdb publication page