PAFAH1B2 c.411+711A>G

Variant ID: 11-117035319-A-G

NM_002572.3(PAFAH1B2):c.411+711A>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Multiple genotype-phenotype association study reveals intronic variant pair on SIDT2 associated with metabolic syndrome in a Korean population.

Human Genomics
Moon, Sanghoon S; Lee, Young Y; Won, Sungho S; Lee, Juyoung J
Publication Date: 2018-11-01

Variant appearance in text: rs12420127
PubMed Link: 30382898
Variant Present in the following documents:
  • Main text
View BVdb publication page



Multiple susceptibility loci at chromosome 11q23.3 are associated with plasma triglyceride in East Asians.

Journal Of Lipid Research
Gombojav, Bayasgalan B; Lee, Soo Ji SJ; Kho, Minjung M; Song, Yun-Mi YM; Lee, Kayoung K; Sung, Joohon J
Publication Date: 2016-02

Variant appearance in text: rs12420127
PubMed Link: 26634697
Variant Present in the following documents:
  • Main text
View BVdb publication page