BATF c.168+9863T>C

Variant ID: 14-76001394-T-C

NM_006399.3(BATF):c.168+9863T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions.

Plos Genetics
Raychaudhuri, Soumya S; Plenge, Robert M RM; Rossin, Elizabeth J EJ; Ng, Aylwin C Y AC; , ; Purcell, Shaun M SM; Sklar, Pamela P; Scolnick, Edward M EM; Xavier, Ramnik J RJ; Altshuler, David D; Daly, Mark J MJ
Publication Date: 2009-06

Variant appearance in text: rs7161377
PubMed Link: 19557189
Variant Present in the following documents:
  • Main text
  • pgen.1000534.pdf
View BVdb publication page