ATP6V1E1 c.530+1442A>G

Variant ID: 22-18079518-T-C

NM_001696.3(ATP6V1E1):c.530+1442A>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease.

Plos One
Östensson, Malin M; Montén, Caroline C; Bacelis, Jonas J; Gudjonsdottir, Audur H AH; Adamovic, Svetlana S; Ek, Johan J; Ascher, Henry H; Pollak, Elisabet E; Arnell, Henrik H; Browaldh, Lars L; Agardh, Daniel D; Wahlström, Jan J; Nilsson, Staffan S; Torinsson-Naluai, Åsa Å
Publication Date: 2013

Variant appearance in text: rs1296826
PubMed Link: 23936387
Variant Present in the following documents:
  • Main text
  • pone.0070174.pdf
View BVdb publication page