GALNT2 c.374+7793C>T

Variant ID: 1-230346829-C-T

NM_004481.3(GALNT2):c.374+7793C>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Re-sequencing expands our understanding of the phenotypic impact of variants at GWAS loci.

Plos Genetics
Service, Susan K SK; Teslovich, Tanya M TM; Fuchsberger, Christian C; Ramensky, Vasily V; Yajnik, Pranav P; Koboldt, Daniel C DC; Larson, David E DE; Zhang, Qunyuan Q; Lin, Ling L; Welch, Ryan R; Ding, Li L; McLellan, Michael D MD; O'Laughlin, Michele M; Fronick, Catrina C; Fulton, Lucinda L LL; Magrini, Vincent V; Swift, Amy A; Elliott, Paul P; Jarvelin, Marjo-Riitta MR; Kaakinen, Marika M; McCarthy, Mark I MI; Peltonen, Leena L; Pouta, Anneli A; Bonnycastle, Lori L LL; Collins, Francis S FS; Narisu, Narisu N; Stringham, Heather M HM; Tuomilehto, Jaakko J; Ripatti, Samuli S; Fulton, Robert S RS; Sabatti, Chiara C; Wilson, Richard K RK; Boehnke, Michael M; Freimer, Nelson B NB
Publication Date: 2014-01

Variant appearance in text: rs4846930
PubMed Link: 24497850
Variant Present in the following documents:
  • Main text
  • pgen.1004147.pdf
View BVdb publication page



Knowledge-driven multi-locus analysis reveals gene-gene interactions influencing HDL cholesterol level in two independent EMR-linked biobanks.

Plos One
Turner, Stephen D SD; Berg, Richard L RL; Linneman, James G JG; Peissig, Peggy L PL; Crawford, Dana C DC; Denny, Joshua C JC; Roden, Dan M DM; McCarty, Catherine A CA; Ritchie, Marylyn D MD; Wilke, Russell A RA
Publication Date: 2011-05-11

Variant appearance in text: rs4846930
PubMed Link: 21589926
Variant Present in the following documents:
  • Main text
  • pone.0019586.pdf
View BVdb publication page