Variant ID: 1-55514182-T-C

NM_174936.3(PCSK9):c.523+1863T>C

This variant was identified in 2 publications




Publications:


Lipid lowering and Alzheimer disease risk: A mendelian randomization study.

Annals Of Neurology
DM Williams, C Finan, AF Schmidt, S Burgess, AD Hingorani
Publication Date: 2020-01

Variant appearance in text: rs535471
PubMed Link: 31714636
Variant Present in the following documents:
  • ANA-87-30-s001.docx
View BVdb publication page



Genetic variability within the cholesterol lowering pathway and the effectiveness of statins in reducing the risk of MI.

Atherosclerosis
BJ Peters, H Pett, OH Klungel, BH Stricker, BM Psaty, NL Glazer, KL Wiggins, JC Bis, A de Boer, AH Maitland-van der Zee
Publication Date: 2011-08

Variant appearance in text: rs535471
PubMed Link: 21741043
Variant Present in the following documents:
  • NIHMS310676-supplement-01.doc
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000302118.5 c.523+1863T>C - intron_variant - 3/11
ENST00000452118.2 c.523+1863T>C - intron_variant - 3/5
ENST00000543384.1 c.-77-3769T>C - intron_variant - 1/9
NM_174936.4 c.523+1863T>C - intron_variant - 3/11
NR_110451.1 n.183-3769T>C - intron_variant,non_coding_transcript_variant - 1/9