NACC2 c.-59-4741T>C

Variant ID: 9-138947167-A-G

NM_144653.4(NACC2):c.-59-4741T>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genetics and epigenetics in primary Sjögren's syndrome.

Rheumatology (Oxford, England)
Imgenberg-Kreuz, Juliana J; Rasmussen, Astrid A; Sivils, Kathy K; Nordmark, Gunnel G
Publication Date: 2021-05-14

Variant appearance in text: rs4842091
PubMed Link: 30770922
Variant Present in the following documents:
  • Main text
  • key330.pdf
View BVdb publication page



Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry.

Arthritis & Rheumatology (Hoboken, N.J.)
Taylor, Kimberly E KE; Wong, Quenna Q; Levine, David M DM; McHugh, Caitlin C; Laurie, Cathy C; Doheny, Kimberly K; Lam, Mi Y MY; Baer, Alan N AN; Challacombe, Stephen S; Lanfranchi, Hector H; Schiødt, Morten M; Srinivasan, M M; Umehara, Hisanori H; Vivino, Frederick B FB; Zhao, Yan Y; Shiboski, Stephen C SC; Daniels, Troy E TE; Greenspan, John S JS; Shiboski, Caroline H CH; Criswell, Lindsey A LA
Publication Date: 2017-06

Variant appearance in text: rs4842091
PubMed Link: 28076899
Variant Present in the following documents:
  • Main text
  • ART-69-1294.pdf
View BVdb publication page