ANKRD17 c.548-6499C>G

Variant ID: 4-74033564-G-C

NM_032217.3(ANKRD17):c.548-6499C>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Association of structural variation with cardiometabolic traits in Finns.

American Journal Of Human Genetics
Chen, Lei L; Abel, Haley J HJ; Das, Indraniel I; Larson, David E DE; Ganel, Liron L; Kanchi, Krishna L KL; Regier, Allison A AA; Young, Erica P EP; Kang, Chul Joo CJ; Scott, Alexandra J AJ; Chiang, Colby C; Wang, Xinxin X; Lu, Shuangjia S; Christ, Ryan R; Service, Susan K SK; Chiang, Charleston W K CWK; Havulinna, Aki S AS; Kuusisto, Johanna J; Boehnke, Michael M; Laakso, Markku M; Palotie, Aarno A; Ripatti, Samuli S; Freimer, Nelson B NB; Locke, Adam E AE; Stitziel, Nathan O NO; Hall, Ira M IM
Publication Date: 2021-04-01

Variant appearance in text: rs187918276
PubMed Link: 33798444
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.

Plos Genetics
Davis, James P JP; Huyghe, Jeroen R JR; Locke, Adam E AE; Jackson, Anne U AU; Sim, Xueling X; Stringham, Heather M HM; Teslovich, Tanya M TM; Welch, Ryan P RP; Fuchsberger, Christian C; Narisu, Narisu N; Chines, Peter S PS; Kangas, Antti J AJ; Soininen, Pasi P; Ala-Korpela, Mika M; Kuusisto, Johanna J; Collins, Francis S FS; Laakso, Markku M; Boehnke, Michael M; Mohlke, Karen L KL
Publication Date: 2017-10

Variant appearance in text: rs187918276
PubMed Link: 29084231
Variant Present in the following documents:
  • Main text
  • pgen.1007079.pdf
View BVdb publication page