NFIA c.626-6321G>A

Variant ID: 1-61791863-G-A

NM_001134673.3(NFIA):c.626-6321G>A

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Independent and cumulative coeliac disease-susceptibility loci are associated with distinct disease phenotypes.

Journal Of Human Genetics
Cerqueira, Juliana X M JXM; Saavalainen, Päivi P; Kurppa, Kalle K; Laurikka, Pilvi P; Huhtala, Heini H; Nykter, Matti M; L E Koskinen, Lotta L; Yohannes, Dawit A DA; Kilpeläinen, Elina E; Shcherban, Anastasia A; Palotie, Aarno A; Kaukinen, Katri K; Lindfors, Katri K
Publication Date: 2021-06

Variant appearance in text: rs6691768
PubMed Link: 33446885
Variant Present in the following documents:
  • 10038_2020_888_MOESM2_ESM.xlsx, sheet 1
  • 10038_2020_888_MOESM3_ESM.xlsx, sheet 1
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Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci.

European Journal Of Human Genetics : Ejhg
Coleman, Ciara C; Quinn, Emma M EM; Ryan, Anthony W AW; Conroy, Judith J; Trimble, Valerie V; Mahmud, Nasir N; Kennedy, Nicholas N; Corvin, Aiden P AP; Morris, Derek W DW; Donohoe, Gary G; O'Morain, Colm C; MacMathuna, Padraic P; Byrnes, Valerie V; Kiat, Clifford C; Trynka, Gosia G; Wijmenga, Cisca C; Kelleher, Dermot D; Ennis, Sean S; Anney, Richard J L RJ; McManus, Ross R
Publication Date: 2016-02

Variant appearance in text: rs6691768
PubMed Link: 25920553
Variant Present in the following documents:
  • Main text
View BVdb publication page



A pleiotropy-informed Bayesian false discovery rate adapted to a shared control design finds new disease associations from GWAS summary statistics.

Plos Genetics
Liley, James J; Wallace, Chris C
Publication Date: 2015-02

Variant appearance in text: rs6691768
PubMed Link: 25658688
Variant Present in the following documents:
  • Main text
  • pgen.1004926.pdf
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Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease.

Nature Genetics
Trynka, Gosia G; Hunt, Karen A KA; Bockett, Nicholas A NA; Romanos, Jihane J; Mistry, Vanisha V; Szperl, Agata A; Bakker, Sjoerd F SF; Bardella, Maria Teresa MT; Bhaw-Rosun, Leena L; Castillejo, Gemma G; de la Concha, Emilio G EG; de Almeida, Rodrigo Coutinho RC; Dias, Kerith-Rae M KR; van Diemen, Cleo C CC; Dubois, Patrick C A PC; Duerr, Richard H RH; Edkins, Sarah S; Franke, Lude L; Fransen, Karin K; Gutierrez, Javier J; Heap, Graham A R GA; Hrdlickova, Barbara B; Hunt, Sarah S; Plaza Izurieta, Leticia L; Izzo, Valentina V; Joosten, Leo A B LA; Langford, Cordelia C; Mazzilli, Maria Cristina MC; Mein, Charles A CA; Midah, Vandana V; Mitrovic, Mitja M; Mora, Barbara B; Morelli, Marinita M; Nutland, Sarah S; Núñez, Concepción C; Onengut-Gumuscu, Suna S; Pearce, Kerra K; Platteel, Mathieu M; Polanco, Isabel I; Potter, Simon S; Ribes-Koninckx, Carmen C; Ricaño-Ponce, Isis I; Rich, Stephen S SS; Rybak, Anna A; Santiago, José Luis JL; Senapati, Sabyasachi S; Sood, Ajit A; Szajewska, Hania H; Troncone, Riccardo R; Varadé, Jezabel J; Wallace, Chris C; Wolters, Victorien M VM; Zhernakova, Alexandra A; , ; , ; , ; Thelma, B K BK; Cukrowska, Bozena B; Urcelay, Elena E; Bilbao, Jose Ramon JR; Mearin, M Luisa ML; Barisani, Donatella D; Barrett, Jeffrey C JC; Plagnol, Vincent V; Deloukas, Panos P; Wijmenga, Cisca C; van Heel, David A DA
Publication Date: 2011-11-06

Variant appearance in text: rs6691768
PubMed Link: 22057235
Variant Present in the following documents:
  • Main text
  • ukmss-37096.pdf
View BVdb publication page



Multiple common variants for celiac disease influencing immune gene expression.

Nature Genetics
Dubois, Patrick C A PC; Trynka, Gosia G; Franke, Lude L; Hunt, Karen A KA; Romanos, Jihane J; Curtotti, Alessandra A; Zhernakova, Alexandra A; Heap, Graham A R GA; Adány, Róza R; Aromaa, Arpo A; Bardella, Maria Teresa MT; van den Berg, Leonard H LH; Bockett, Nicholas A NA; de la Concha, Emilio G EG; Dema, Bárbara B; Fehrmann, Rudolf S N RS; Fernández-Arquero, Miguel M; Fiatal, Szilvia S; Grandone, Elvira E; Green, Peter M PM; Groen, Harry J M HJ; Gwilliam, Rhian R; Houwen, Roderick H J RH; Hunt, Sarah E SE; Kaukinen, Katri K; Kelleher, Dermot D; Korponay-Szabo, Ilma I; Kurppa, Kalle K; MacMathuna, Padraic P; Mäki, Markku M; Mazzilli, Maria Cristina MC; McCann, Owen T OT; Mearin, M Luisa ML; Mein, Charles A CA; Mirza, Muddassar M MM; Mistry, Vanisha V; Mora, Barbara B; Morley, Katherine I KI; Mulder, Chris J CJ; Murray, Joseph A JA; Núñez, Concepción C; Oosterom, Elvira E; Ophoff, Roel A RA; Polanco, Isabel I; Peltonen, Leena L; Platteel, Mathieu M; Rybak, Anna A; Salomaa, Veikko V; Schweizer, Joachim J JJ; Sperandeo, Maria Pia MP; Tack, Greetje J GJ; Turner, Graham G; Veldink, Jan H JH; Verbeek, Wieke H M WH; Weersma, Rinse K RK; Wolters, Victorien M VM; Urcelay, Elena E; Cukrowska, Bozena B; Greco, Luigi L; Neuhausen, Susan L SL; McManus, Ross R; Barisani, Donatella D; Deloukas, Panos P; Barrett, Jeffrey C JC; Saavalainen, Paivi P; Wijmenga, Cisca C; van Heel, David A DA
Publication Date: 2010-04

Variant appearance in text: rs6691768
PubMed Link: 20190752
Variant Present in the following documents:
  • Main text
View BVdb publication page