PCSK9 c.207+1568T>C

Variant ID: 1-55507285-T-C

NM_174936.3(PCSK9):c.207+1568T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Lipids, obesity and gallbladder disease in women: insights from genetic studies using the cardiovascular gene-centric 50K SNP array.

European Journal Of Human Genetics : Ejhg
Rodriguez, Santiago S; Gaunt, Tom R TR; Guo, Yiran Y; Zheng, Jie J; Barnes, Michael R MR; Tang, Weihang W; Danish, Fazal F; Johnson, Andrew A; Castillo, Berta A BA; Li, Yun R YR; Hakonarson, Hakon H; Buxbaum, Sarah G SG; Palmer, Tom T; Tsai, Michael Y MY; Lange, Leslie A LA; Ebrahim, Shah S; Davey Smith, George G; Lawlor, Debbie A DA; Folsom, Aaron R AR; Hoogeveen, Ron R; Reiner, Alex A; Keating, Brendan B; Day, Ian N M IN
Publication Date: 2016-01

Variant appearance in text: rs28385705
PubMed Link: 25920552
Variant Present in the following documents:
  • Main text
View BVdb publication page