Variant ID: 1-55513169-T-G

NM_174936.3(PCSK9):c.523+850T>G

This variant was identified in 1 publication




Publications:


Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.

Plos Genetics
G Lettre, CD Palmer, T Young, KG Ejebe, H Allayee, EJ Benjamin, F Bennett, DW Bowden, A Chakravarti, A Dreisbach, DN Farlow, AR Folsom, M Fornage, T Forrester, E Fox, CA Haiman, J Hartiala, TB Harris, SL Hazen, SR Heckbert, BE Henderson, JN Hirschhorn, BJ Keating, SB Kritchevsky, E Larkin, M Li, ME Rudock, CA McKenzie, JB Meigs, YA Meng, TH Mosley, AB Newman, CH Newton-Cheh, DN Paltoo, GJ Papanicolaou, N Patterson, WS Post, BM Psaty, AN Qasim, L Qu, DJ Rader, S Redline, MP Reilly, AP Reiner, SS Rich, JI Rotter, Y Liu, P Shrader, DS Siscovick, WH Tang, HA Taylor, RP Tracy, RS Vasan, KM Waters, R Wilks, JG Wilson, RR Fabsitz, SB Gabriel, S Kathiresan, E Boerwinkle
Publication Date: 2011-02-10

Variant appearance in text: rs12066265
PubMed Link: 21347282
Variant Present in the following documents:
  • pgen.1001300.s011.doc
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.523+850T>G - intron_variant - 3/11
ENST00000452118.2 c.523+850T>G - intron_variant - 3/5
ENST00000543384.1 c.-77-4782T>G - intron_variant - 1/9
NM_174936.4 c.523+850T>G - intron_variant - 3/11
NR_110451.1 n.183-4782T>G - intron_variant,non_coding_transcript_variant - 1/9