RELN c.545-10305T>C

Variant ID: 7-103403966-A-G

NM_005045.3(RELN):c.545-10305T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


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: rs73180120
PubMed Link: 28076899
Variant Present in the following documents:
  • Main text
  • ART-69-1294.pdf
View BVdb publication page